Name: rs11288108
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs11288108

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:72937411-72937430 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₁ / del(T)₁₀ / del(T)₈ / de…
del(T)₁₁ / del(T)₁₀ / del(T)₈ / del(T)₇ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / ins(T)₂₉ / ins(T)₃₃
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₈=0.000008 (2/264690, TOPMED)
dupTT=0.1825 (1050/5754, ALFA)
dupTT=0.47 (19/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DCAF4 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	5754	TTTTTTTTTTTTTTTTTTTT=0.5733	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0718, TTTTTTTTTTTTTTTTTTTTT=0.1500, TTTTTTTTTTTTTTTTTTTTTT=0.1825, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0127, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0075, TTTTTTTTTTTTTTTTTTTTTTT=0.0023, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.779435	0.153969	0.066596	32
European	Sub	4998	TTTTTTTTTTTTTTTTTTTT=0.5098	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0824, TTTTTTTTTTTTTTTTTTTTT=0.1725, TTTTTTTTTTTTTTTTTTTTTT=0.2095, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0146, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0086, TTTTTTTTTTTTTTTTTTTTTTT=0.0026, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.72485	0.191872	0.083278	32
African	Sub	642	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	26	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	616	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	4	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	14	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	22	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	14	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	60	TTTTTTTTTTTTTTTTTTTT=0.92	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.02, TTTTTTTTTTTTTTTTTTTTT=0.02, TTTTTTTTTTTTTTTTTTTTTT=0.05, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.964286	0.035714	0.0	15

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(T)₂₀=0.999992	del(T)₈=0.000008
Allele Frequency Aggregator	Total	Global	5754	(T)₂₀=0.5733	del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0718, dupT=0.1500, dupTT=0.1825, dupTTT=0.0023, dup(T)₄=0.0000, dup(T)₆=0.0075, dup(T)₇=0.0127
Allele Frequency Aggregator	European	Sub	4998	(T)₂₀=0.5098	del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0824, dupT=0.1725, dupTT=0.2095, dupTTT=0.0026, dup(T)₄=0.0000, dup(T)₆=0.0086, dup(T)₇=0.0146
Allele Frequency Aggregator	African	Sub	642	(T)₂₀=1.000	del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Other	Sub	60	(T)₂₀=0.92	del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.02, dupT=0.02, dupTT=0.05, dupTTT=0.00, dup(T)₄=0.00, dup(T)₆=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	Latin American 2	Sub	22	(T)₂₀=1.00	del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₆=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	Latin American 1	Sub	14	(T)₂₀=1.00	del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₆=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	14	(T)₂₀=1.00	del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₆=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	Asian	Sub	4	(T)₂₀=1.0	del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₆=0.0, dup(T)₇=0.0
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupTT=0.47

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 14	NC_000014.9:g.72937420_72937430del
GRCh38.p14 chr 14	NC_000014.9:g.72937421_72937430del
GRCh38.p14 chr 14	NC_000014.9:g.72937423_72937430del
GRCh38.p14 chr 14	NC_000014.9:g.72937424_72937430del
GRCh38.p14 chr 14	NC_000014.9:g.72937426_72937430del
GRCh38.p14 chr 14	NC_000014.9:g.72937427_72937430del
GRCh38.p14 chr 14	NC_000014.9:g.72937428_72937430del
GRCh38.p14 chr 14	NC_000014.9:g.72937429_72937430del
GRCh38.p14 chr 14	NC_000014.9:g.72937430del
GRCh38.p14 chr 14	NC_000014.9:g.72937430dup
GRCh38.p14 chr 14	NC_000014.9:g.72937429_72937430dup
GRCh38.p14 chr 14	NC_000014.9:g.72937428_72937430dup
GRCh38.p14 chr 14	NC_000014.9:g.72937427_72937430dup
GRCh38.p14 chr 14	NC_000014.9:g.72937426_72937430dup
GRCh38.p14 chr 14	NC_000014.9:g.72937425_72937430dup
GRCh38.p14 chr 14	NC_000014.9:g.72937424_72937430dup
GRCh38.p14 chr 14	NC_000014.9:g.72937423_72937430dup
GRCh38.p14 chr 14	NC_000014.9:g.72937422_72937430dup
GRCh38.p14 chr 14	NC_000014.9:g.72937421_72937430dup
GRCh38.p14 chr 14	NC_000014.9:g.72937420_72937430dup
GRCh38.p14 chr 14	NC_000014.9:g.72937419_72937430dup
GRCh38.p14 chr 14	NC_000014.9:g.72937430_72937431insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 14	NC_000014.9:g.72937430_72937431insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 14	NC_000014.8:g.73404128_73404138del
GRCh37.p13 chr 14	NC_000014.8:g.73404129_73404138del
GRCh37.p13 chr 14	NC_000014.8:g.73404131_73404138del
GRCh37.p13 chr 14	NC_000014.8:g.73404132_73404138del
GRCh37.p13 chr 14	NC_000014.8:g.73404134_73404138del
GRCh37.p13 chr 14	NC_000014.8:g.73404135_73404138del
GRCh37.p13 chr 14	NC_000014.8:g.73404136_73404138del
GRCh37.p13 chr 14	NC_000014.8:g.73404137_73404138del
GRCh37.p13 chr 14	NC_000014.8:g.73404138del
GRCh37.p13 chr 14	NC_000014.8:g.73404138dup
GRCh37.p13 chr 14	NC_000014.8:g.73404137_73404138dup
GRCh37.p13 chr 14	NC_000014.8:g.73404136_73404138dup
GRCh37.p13 chr 14	NC_000014.8:g.73404135_73404138dup
GRCh37.p13 chr 14	NC_000014.8:g.73404134_73404138dup
GRCh37.p13 chr 14	NC_000014.8:g.73404133_73404138dup
GRCh37.p13 chr 14	NC_000014.8:g.73404132_73404138dup
GRCh37.p13 chr 14	NC_000014.8:g.73404131_73404138dup
GRCh37.p13 chr 14	NC_000014.8:g.73404130_73404138dup
GRCh37.p13 chr 14	NC_000014.8:g.73404129_73404138dup
GRCh37.p13 chr 14	NC_000014.8:g.73404128_73404138dup
GRCh37.p13 chr 14	NC_000014.8:g.73404127_73404138dup
GRCh37.p13 chr 14	NC_000014.8:g.73404138_73404139insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 14	NC_000014.8:g.73404138_73404139insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 RefSeqGene	NG_047140.1:g.16089_16099del
DCAF4 RefSeqGene	NG_047140.1:g.16090_16099del
DCAF4 RefSeqGene	NG_047140.1:g.16092_16099del
DCAF4 RefSeqGene	NG_047140.1:g.16093_16099del
DCAF4 RefSeqGene	NG_047140.1:g.16095_16099del
DCAF4 RefSeqGene	NG_047140.1:g.16096_16099del
DCAF4 RefSeqGene	NG_047140.1:g.16097_16099del
DCAF4 RefSeqGene	NG_047140.1:g.16098_16099del
DCAF4 RefSeqGene	NG_047140.1:g.16099del
DCAF4 RefSeqGene	NG_047140.1:g.16099dup
DCAF4 RefSeqGene	NG_047140.1:g.16098_16099dup
DCAF4 RefSeqGene	NG_047140.1:g.16097_16099dup
DCAF4 RefSeqGene	NG_047140.1:g.16096_16099dup
DCAF4 RefSeqGene	NG_047140.1:g.16095_16099dup
DCAF4 RefSeqGene	NG_047140.1:g.16094_16099dup
DCAF4 RefSeqGene	NG_047140.1:g.16093_16099dup
DCAF4 RefSeqGene	NG_047140.1:g.16092_16099dup
DCAF4 RefSeqGene	NG_047140.1:g.16091_16099dup
DCAF4 RefSeqGene	NG_047140.1:g.16090_16099dup
DCAF4 RefSeqGene	NG_047140.1:g.16089_16099dup
DCAF4 RefSeqGene	NG_047140.1:g.16088_16099dup
DCAF4 RefSeqGene	NG_047140.1:g.16099_16100insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 RefSeqGene	NG_047140.1:g.16099_16100insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: DCAF4, DDB1 and CUL4 associated factor 4 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DCAF4 transcript variant 4	NM_001163508.2:c.-8-551_-… NM_001163508.2:c.-8-551_-8-541del	N/A	Intron Variant
DCAF4 transcript variant 5	NM_001163509.2:c.-42-551_… NM_001163509.2:c.-42-551_-42-541del	N/A	Intron Variant
DCAF4 transcript variant 6	NM_001352447.2:c.-649-551… NM_001352447.2:c.-649-551_-649-541del	N/A	Intron Variant
DCAF4 transcript variant 7	NM_001352448.3:c.-8-551_-… NM_001352448.3:c.-8-551_-8-541del	N/A	Intron Variant
DCAF4 transcript variant 8	NM_001352449.2:c.-8-551_-… NM_001352449.2:c.-8-551_-8-541del	N/A	Intron Variant
DCAF4 transcript variant 1	NM_015604.4:c.-8-551_-8-5… NM_015604.4:c.-8-551_-8-541del	N/A	Intron Variant
DCAF4 transcript variant 2	NM_181340.3:c.-208-2382_-… NM_181340.3:c.-208-2382_-208-2372del	N/A	Intron Variant
DCAF4 transcript variant 3	NM_181341.3:c.-8-551_-8-5… NM_181341.3:c.-8-551_-8-541del	N/A	Intron Variant
DCAF4 transcript variant 9	NR_147990.2:n.	N/A	Intron Variant
DCAF4 transcript variant X7	XM_017021205.2:c.-8-551_-… XM_017021205.2:c.-8-551_-8-541del	N/A	Intron Variant
DCAF4 transcript variant X8	XM_017021206.2:c.-8-551_-… XM_017021206.2:c.-8-551_-8-541del	N/A	Intron Variant
DCAF4 transcript variant X10	XM_017021213.3:c.-42-551_… XM_017021213.3:c.-42-551_-42-541del	N/A	Intron Variant
DCAF4 transcript variant X2	XM_047431254.1:c.65-551_6… XM_047431254.1:c.65-551_65-541del	N/A	Intron Variant
DCAF4 transcript variant X3	XM_047431255.1:c.65-551_6… XM_047431255.1:c.65-551_65-541del	N/A	Intron Variant
DCAF4 transcript variant X5	XM_047431256.1:c.65-551_6… XM_047431256.1:c.65-551_65-541del	N/A	Intron Variant
DCAF4 transcript variant X6	XM_047431257.1:c.65-551_6… XM_047431257.1:c.65-551_65-541del	N/A	Intron Variant
DCAF4 transcript variant X9	XM_047431258.1:c.-42-551_… XM_047431258.1:c.-42-551_-42-541del	N/A	Intron Variant
DCAF4 transcript variant X11	XM_047431259.1:c.-42-551_… XM_047431259.1:c.-42-551_-42-541del	N/A	Intron Variant
DCAF4 transcript variant X12	XM_047431260.1:c.-42-551_… XM_047431260.1:c.-42-551_-42-541del	N/A	Intron Variant
DCAF4 transcript variant X4	XR_007064003.1:n.	N/A	Intron Variant
DCAF4 transcript variant X1	XR_007064002.1:n.	N/A	Genic Upstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₀=	del(T)₁₁	del(T)₁₀	del(T)₈	del(T)₇	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	ins(T)₂₉	ins(T)₃₃
GRCh38.p14 chr 14	NC_000014.9:g.72937411_72937430=	NC_000014.9:g.72937420_72937430del	NC_000014.9:g.72937421_72937430del	NC_000014.9:g.72937423_72937430del	NC_000014.9:g.72937424_72937430del	NC_000014.9:g.72937426_72937430del	NC_000014.9:g.72937427_72937430del	NC_000014.9:g.72937428_72937430del	NC_000014.9:g.72937429_72937430del	NC_000014.9:g.72937430del	NC_000014.9:g.72937430dup	NC_000014.9:g.72937429_72937430dup	NC_000014.9:g.72937428_72937430dup	NC_000014.9:g.72937427_72937430dup	NC_000014.9:g.72937426_72937430dup	NC_000014.9:g.72937425_72937430dup	NC_000014.9:g.72937424_72937430dup	NC_000014.9:g.72937423_72937430dup	NC_000014.9:g.72937422_72937430dup	NC_000014.9:g.72937421_72937430dup	NC_000014.9:g.72937420_72937430dup	NC_000014.9:g.72937419_72937430dup	NC_000014.9:g.72937430_72937431insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:g.72937430_72937431insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 14	NC_000014.8:g.73404119_73404138=	NC_000014.8:g.73404128_73404138del	NC_000014.8:g.73404129_73404138del	NC_000014.8:g.73404131_73404138del	NC_000014.8:g.73404132_73404138del	NC_000014.8:g.73404134_73404138del	NC_000014.8:g.73404135_73404138del	NC_000014.8:g.73404136_73404138del	NC_000014.8:g.73404137_73404138del	NC_000014.8:g.73404138del	NC_000014.8:g.73404138dup	NC_000014.8:g.73404137_73404138dup	NC_000014.8:g.73404136_73404138dup	NC_000014.8:g.73404135_73404138dup	NC_000014.8:g.73404134_73404138dup	NC_000014.8:g.73404133_73404138dup	NC_000014.8:g.73404132_73404138dup	NC_000014.8:g.73404131_73404138dup	NC_000014.8:g.73404130_73404138dup	NC_000014.8:g.73404129_73404138dup	NC_000014.8:g.73404128_73404138dup	NC_000014.8:g.73404127_73404138dup	NC_000014.8:g.73404138_73404139insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.8:g.73404138_73404139insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 RefSeqGene	NG_047140.1:g.16080_16099=	NG_047140.1:g.16089_16099del	NG_047140.1:g.16090_16099del	NG_047140.1:g.16092_16099del	NG_047140.1:g.16093_16099del	NG_047140.1:g.16095_16099del	NG_047140.1:g.16096_16099del	NG_047140.1:g.16097_16099del	NG_047140.1:g.16098_16099del	NG_047140.1:g.16099del	NG_047140.1:g.16099dup	NG_047140.1:g.16098_16099dup	NG_047140.1:g.16097_16099dup	NG_047140.1:g.16096_16099dup	NG_047140.1:g.16095_16099dup	NG_047140.1:g.16094_16099dup	NG_047140.1:g.16093_16099dup	NG_047140.1:g.16092_16099dup	NG_047140.1:g.16091_16099dup	NG_047140.1:g.16090_16099dup	NG_047140.1:g.16089_16099dup	NG_047140.1:g.16088_16099dup	NG_047140.1:g.16099_16100insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NG_047140.1:g.16099_16100insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant 4	NM_001163508.1:c.-8-560=	NM_001163508.1:c.-8-551_-8-541del	NM_001163508.1:c.-8-550_-8-541del	NM_001163508.1:c.-8-548_-8-541del	NM_001163508.1:c.-8-547_-8-541del	NM_001163508.1:c.-8-545_-8-541del	NM_001163508.1:c.-8-544_-8-541del	NM_001163508.1:c.-8-543_-8-541del	NM_001163508.1:c.-8-542_-8-541del	NM_001163508.1:c.-8-541del	NM_001163508.1:c.-8-541dup	NM_001163508.1:c.-8-542_-8-541dup	NM_001163508.1:c.-8-543_-8-541dup	NM_001163508.1:c.-8-544_-8-541dup	NM_001163508.1:c.-8-545_-8-541dup	NM_001163508.1:c.-8-546_-8-541dup	NM_001163508.1:c.-8-547_-8-541dup	NM_001163508.1:c.-8-548_-8-541dup	NM_001163508.1:c.-8-549_-8-541dup	NM_001163508.1:c.-8-550_-8-541dup	NM_001163508.1:c.-8-551_-8-541dup	NM_001163508.1:c.-8-552_-8-541dup	NM_001163508.1:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001163508.1:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant 4	NM_001163508.2:c.-8-560=	NM_001163508.2:c.-8-551_-8-541del	NM_001163508.2:c.-8-550_-8-541del	NM_001163508.2:c.-8-548_-8-541del	NM_001163508.2:c.-8-547_-8-541del	NM_001163508.2:c.-8-545_-8-541del	NM_001163508.2:c.-8-544_-8-541del	NM_001163508.2:c.-8-543_-8-541del	NM_001163508.2:c.-8-542_-8-541del	NM_001163508.2:c.-8-541del	NM_001163508.2:c.-8-541dup	NM_001163508.2:c.-8-542_-8-541dup	NM_001163508.2:c.-8-543_-8-541dup	NM_001163508.2:c.-8-544_-8-541dup	NM_001163508.2:c.-8-545_-8-541dup	NM_001163508.2:c.-8-546_-8-541dup	NM_001163508.2:c.-8-547_-8-541dup	NM_001163508.2:c.-8-548_-8-541dup	NM_001163508.2:c.-8-549_-8-541dup	NM_001163508.2:c.-8-550_-8-541dup	NM_001163508.2:c.-8-551_-8-541dup	NM_001163508.2:c.-8-552_-8-541dup	NM_001163508.2:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001163508.2:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant 5	NM_001163509.1:c.-42-560=	NM_001163509.1:c.-42-551_-42-541del	NM_001163509.1:c.-42-550_-42-541del	NM_001163509.1:c.-42-548_-42-541del	NM_001163509.1:c.-42-547_-42-541del	NM_001163509.1:c.-42-545_-42-541del	NM_001163509.1:c.-42-544_-42-541del	NM_001163509.1:c.-42-543_-42-541del	NM_001163509.1:c.-42-542_-42-541del	NM_001163509.1:c.-42-541del	NM_001163509.1:c.-42-541dup	NM_001163509.1:c.-42-542_-42-541dup	NM_001163509.1:c.-42-543_-42-541dup	NM_001163509.1:c.-42-544_-42-541dup	NM_001163509.1:c.-42-545_-42-541dup	NM_001163509.1:c.-42-546_-42-541dup	NM_001163509.1:c.-42-547_-42-541dup	NM_001163509.1:c.-42-548_-42-541dup	NM_001163509.1:c.-42-549_-42-541dup	NM_001163509.1:c.-42-550_-42-541dup	NM_001163509.1:c.-42-551_-42-541dup	NM_001163509.1:c.-42-552_-42-541dup	NM_001163509.1:c.-42-541_-42-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001163509.1:c.-42-541_-42-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant 5	NM_001163509.2:c.-42-560=	NM_001163509.2:c.-42-551_-42-541del	NM_001163509.2:c.-42-550_-42-541del	NM_001163509.2:c.-42-548_-42-541del	NM_001163509.2:c.-42-547_-42-541del	NM_001163509.2:c.-42-545_-42-541del	NM_001163509.2:c.-42-544_-42-541del	NM_001163509.2:c.-42-543_-42-541del	NM_001163509.2:c.-42-542_-42-541del	NM_001163509.2:c.-42-541del	NM_001163509.2:c.-42-541dup	NM_001163509.2:c.-42-542_-42-541dup	NM_001163509.2:c.-42-543_-42-541dup	NM_001163509.2:c.-42-544_-42-541dup	NM_001163509.2:c.-42-545_-42-541dup	NM_001163509.2:c.-42-546_-42-541dup	NM_001163509.2:c.-42-547_-42-541dup	NM_001163509.2:c.-42-548_-42-541dup	NM_001163509.2:c.-42-549_-42-541dup	NM_001163509.2:c.-42-550_-42-541dup	NM_001163509.2:c.-42-551_-42-541dup	NM_001163509.2:c.-42-552_-42-541dup	NM_001163509.2:c.-42-541_-42-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001163509.2:c.-42-541_-42-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant 6	NM_001352447.2:c.-649-560=	NM_001352447.2:c.-649-551_-649-541del	NM_001352447.2:c.-649-550_-649-541del	NM_001352447.2:c.-649-548_-649-541del	NM_001352447.2:c.-649-547_-649-541del	NM_001352447.2:c.-649-545_-649-541del	NM_001352447.2:c.-649-544_-649-541del	NM_001352447.2:c.-649-543_-649-541del	NM_001352447.2:c.-649-542_-649-541del	NM_001352447.2:c.-649-541del	NM_001352447.2:c.-649-541dup	NM_001352447.2:c.-649-542_-649-541dup	NM_001352447.2:c.-649-543_-649-541dup	NM_001352447.2:c.-649-544_-649-541dup	NM_001352447.2:c.-649-545_-649-541dup	NM_001352447.2:c.-649-546_-649-541dup	NM_001352447.2:c.-649-547_-649-541dup	NM_001352447.2:c.-649-548_-649-541dup	NM_001352447.2:c.-649-549_-649-541dup	NM_001352447.2:c.-649-550_-649-541dup	NM_001352447.2:c.-649-551_-649-541dup	NM_001352447.2:c.-649-552_-649-541dup	NM_001352447.2:c.-649-541_-649-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001352447.2:c.-649-541_-649-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant 7	NM_001352448.3:c.-8-560=	NM_001352448.3:c.-8-551_-8-541del	NM_001352448.3:c.-8-550_-8-541del	NM_001352448.3:c.-8-548_-8-541del	NM_001352448.3:c.-8-547_-8-541del	NM_001352448.3:c.-8-545_-8-541del	NM_001352448.3:c.-8-544_-8-541del	NM_001352448.3:c.-8-543_-8-541del	NM_001352448.3:c.-8-542_-8-541del	NM_001352448.3:c.-8-541del	NM_001352448.3:c.-8-541dup	NM_001352448.3:c.-8-542_-8-541dup	NM_001352448.3:c.-8-543_-8-541dup	NM_001352448.3:c.-8-544_-8-541dup	NM_001352448.3:c.-8-545_-8-541dup	NM_001352448.3:c.-8-546_-8-541dup	NM_001352448.3:c.-8-547_-8-541dup	NM_001352448.3:c.-8-548_-8-541dup	NM_001352448.3:c.-8-549_-8-541dup	NM_001352448.3:c.-8-550_-8-541dup	NM_001352448.3:c.-8-551_-8-541dup	NM_001352448.3:c.-8-552_-8-541dup	NM_001352448.3:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001352448.3:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant 8	NM_001352449.2:c.-8-560=	NM_001352449.2:c.-8-551_-8-541del	NM_001352449.2:c.-8-550_-8-541del	NM_001352449.2:c.-8-548_-8-541del	NM_001352449.2:c.-8-547_-8-541del	NM_001352449.2:c.-8-545_-8-541del	NM_001352449.2:c.-8-544_-8-541del	NM_001352449.2:c.-8-543_-8-541del	NM_001352449.2:c.-8-542_-8-541del	NM_001352449.2:c.-8-541del	NM_001352449.2:c.-8-541dup	NM_001352449.2:c.-8-542_-8-541dup	NM_001352449.2:c.-8-543_-8-541dup	NM_001352449.2:c.-8-544_-8-541dup	NM_001352449.2:c.-8-545_-8-541dup	NM_001352449.2:c.-8-546_-8-541dup	NM_001352449.2:c.-8-547_-8-541dup	NM_001352449.2:c.-8-548_-8-541dup	NM_001352449.2:c.-8-549_-8-541dup	NM_001352449.2:c.-8-550_-8-541dup	NM_001352449.2:c.-8-551_-8-541dup	NM_001352449.2:c.-8-552_-8-541dup	NM_001352449.2:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001352449.2:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant 1	NM_015604.3:c.-8-560=	NM_015604.3:c.-8-551_-8-541del	NM_015604.3:c.-8-550_-8-541del	NM_015604.3:c.-8-548_-8-541del	NM_015604.3:c.-8-547_-8-541del	NM_015604.3:c.-8-545_-8-541del	NM_015604.3:c.-8-544_-8-541del	NM_015604.3:c.-8-543_-8-541del	NM_015604.3:c.-8-542_-8-541del	NM_015604.3:c.-8-541del	NM_015604.3:c.-8-541dup	NM_015604.3:c.-8-542_-8-541dup	NM_015604.3:c.-8-543_-8-541dup	NM_015604.3:c.-8-544_-8-541dup	NM_015604.3:c.-8-545_-8-541dup	NM_015604.3:c.-8-546_-8-541dup	NM_015604.3:c.-8-547_-8-541dup	NM_015604.3:c.-8-548_-8-541dup	NM_015604.3:c.-8-549_-8-541dup	NM_015604.3:c.-8-550_-8-541dup	NM_015604.3:c.-8-551_-8-541dup	NM_015604.3:c.-8-552_-8-541dup	NM_015604.3:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_015604.3:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant 1	NM_015604.4:c.-8-560=	NM_015604.4:c.-8-551_-8-541del	NM_015604.4:c.-8-550_-8-541del	NM_015604.4:c.-8-548_-8-541del	NM_015604.4:c.-8-547_-8-541del	NM_015604.4:c.-8-545_-8-541del	NM_015604.4:c.-8-544_-8-541del	NM_015604.4:c.-8-543_-8-541del	NM_015604.4:c.-8-542_-8-541del	NM_015604.4:c.-8-541del	NM_015604.4:c.-8-541dup	NM_015604.4:c.-8-542_-8-541dup	NM_015604.4:c.-8-543_-8-541dup	NM_015604.4:c.-8-544_-8-541dup	NM_015604.4:c.-8-545_-8-541dup	NM_015604.4:c.-8-546_-8-541dup	NM_015604.4:c.-8-547_-8-541dup	NM_015604.4:c.-8-548_-8-541dup	NM_015604.4:c.-8-549_-8-541dup	NM_015604.4:c.-8-550_-8-541dup	NM_015604.4:c.-8-551_-8-541dup	NM_015604.4:c.-8-552_-8-541dup	NM_015604.4:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_015604.4:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant 2	NM_181340.2:c.-208-2391=	NM_181340.2:c.-208-2382_-208-2372del	NM_181340.2:c.-208-2381_-208-2372del	NM_181340.2:c.-208-2379_-208-2372del	NM_181340.2:c.-208-2378_-208-2372del	NM_181340.2:c.-208-2376_-208-2372del	NM_181340.2:c.-208-2375_-208-2372del	NM_181340.2:c.-208-2374_-208-2372del	NM_181340.2:c.-208-2373_-208-2372del	NM_181340.2:c.-208-2372del	NM_181340.2:c.-208-2372dup	NM_181340.2:c.-208-2373_-208-2372dup	NM_181340.2:c.-208-2374_-208-2372dup	NM_181340.2:c.-208-2375_-208-2372dup	NM_181340.2:c.-208-2376_-208-2372dup	NM_181340.2:c.-208-2377_-208-2372dup	NM_181340.2:c.-208-2378_-208-2372dup	NM_181340.2:c.-208-2379_-208-2372dup	NM_181340.2:c.-208-2380_-208-2372dup	NM_181340.2:c.-208-2381_-208-2372dup	NM_181340.2:c.-208-2382_-208-2372dup	NM_181340.2:c.-208-2383_-208-2372dup	NM_181340.2:c.-208-2372_-208-2371insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_181340.2:c.-208-2372_-208-2371insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant 2	NM_181340.3:c.-208-2391=	NM_181340.3:c.-208-2382_-208-2372del	NM_181340.3:c.-208-2381_-208-2372del	NM_181340.3:c.-208-2379_-208-2372del	NM_181340.3:c.-208-2378_-208-2372del	NM_181340.3:c.-208-2376_-208-2372del	NM_181340.3:c.-208-2375_-208-2372del	NM_181340.3:c.-208-2374_-208-2372del	NM_181340.3:c.-208-2373_-208-2372del	NM_181340.3:c.-208-2372del	NM_181340.3:c.-208-2372dup	NM_181340.3:c.-208-2373_-208-2372dup	NM_181340.3:c.-208-2374_-208-2372dup	NM_181340.3:c.-208-2375_-208-2372dup	NM_181340.3:c.-208-2376_-208-2372dup	NM_181340.3:c.-208-2377_-208-2372dup	NM_181340.3:c.-208-2378_-208-2372dup	NM_181340.3:c.-208-2379_-208-2372dup	NM_181340.3:c.-208-2380_-208-2372dup	NM_181340.3:c.-208-2381_-208-2372dup	NM_181340.3:c.-208-2382_-208-2372dup	NM_181340.3:c.-208-2383_-208-2372dup	NM_181340.3:c.-208-2372_-208-2371insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_181340.3:c.-208-2372_-208-2371insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant 3	NM_181341.2:c.-8-560=	NM_181341.2:c.-8-551_-8-541del	NM_181341.2:c.-8-550_-8-541del	NM_181341.2:c.-8-548_-8-541del	NM_181341.2:c.-8-547_-8-541del	NM_181341.2:c.-8-545_-8-541del	NM_181341.2:c.-8-544_-8-541del	NM_181341.2:c.-8-543_-8-541del	NM_181341.2:c.-8-542_-8-541del	NM_181341.2:c.-8-541del	NM_181341.2:c.-8-541dup	NM_181341.2:c.-8-542_-8-541dup	NM_181341.2:c.-8-543_-8-541dup	NM_181341.2:c.-8-544_-8-541dup	NM_181341.2:c.-8-545_-8-541dup	NM_181341.2:c.-8-546_-8-541dup	NM_181341.2:c.-8-547_-8-541dup	NM_181341.2:c.-8-548_-8-541dup	NM_181341.2:c.-8-549_-8-541dup	NM_181341.2:c.-8-550_-8-541dup	NM_181341.2:c.-8-551_-8-541dup	NM_181341.2:c.-8-552_-8-541dup	NM_181341.2:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_181341.2:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant 3	NM_181341.3:c.-8-560=	NM_181341.3:c.-8-551_-8-541del	NM_181341.3:c.-8-550_-8-541del	NM_181341.3:c.-8-548_-8-541del	NM_181341.3:c.-8-547_-8-541del	NM_181341.3:c.-8-545_-8-541del	NM_181341.3:c.-8-544_-8-541del	NM_181341.3:c.-8-543_-8-541del	NM_181341.3:c.-8-542_-8-541del	NM_181341.3:c.-8-541del	NM_181341.3:c.-8-541dup	NM_181341.3:c.-8-542_-8-541dup	NM_181341.3:c.-8-543_-8-541dup	NM_181341.3:c.-8-544_-8-541dup	NM_181341.3:c.-8-545_-8-541dup	NM_181341.3:c.-8-546_-8-541dup	NM_181341.3:c.-8-547_-8-541dup	NM_181341.3:c.-8-548_-8-541dup	NM_181341.3:c.-8-549_-8-541dup	NM_181341.3:c.-8-550_-8-541dup	NM_181341.3:c.-8-551_-8-541dup	NM_181341.3:c.-8-552_-8-541dup	NM_181341.3:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_181341.3:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant X1	XM_005267522.1:c.-8-560=	XM_005267522.1:c.-8-551_-8-541del	XM_005267522.1:c.-8-550_-8-541del	XM_005267522.1:c.-8-548_-8-541del	XM_005267522.1:c.-8-547_-8-541del	XM_005267522.1:c.-8-545_-8-541del	XM_005267522.1:c.-8-544_-8-541del	XM_005267522.1:c.-8-543_-8-541del	XM_005267522.1:c.-8-542_-8-541del	XM_005267522.1:c.-8-541del	XM_005267522.1:c.-8-541dup	XM_005267522.1:c.-8-542_-8-541dup	XM_005267522.1:c.-8-543_-8-541dup	XM_005267522.1:c.-8-544_-8-541dup	XM_005267522.1:c.-8-545_-8-541dup	XM_005267522.1:c.-8-546_-8-541dup	XM_005267522.1:c.-8-547_-8-541dup	XM_005267522.1:c.-8-548_-8-541dup	XM_005267522.1:c.-8-549_-8-541dup	XM_005267522.1:c.-8-550_-8-541dup	XM_005267522.1:c.-8-551_-8-541dup	XM_005267522.1:c.-8-552_-8-541dup	XM_005267522.1:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005267522.1:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant X2	XM_005267523.1:c.-8-560=	XM_005267523.1:c.-8-551_-8-541del	XM_005267523.1:c.-8-550_-8-541del	XM_005267523.1:c.-8-548_-8-541del	XM_005267523.1:c.-8-547_-8-541del	XM_005267523.1:c.-8-545_-8-541del	XM_005267523.1:c.-8-544_-8-541del	XM_005267523.1:c.-8-543_-8-541del	XM_005267523.1:c.-8-542_-8-541del	XM_005267523.1:c.-8-541del	XM_005267523.1:c.-8-541dup	XM_005267523.1:c.-8-542_-8-541dup	XM_005267523.1:c.-8-543_-8-541dup	XM_005267523.1:c.-8-544_-8-541dup	XM_005267523.1:c.-8-545_-8-541dup	XM_005267523.1:c.-8-546_-8-541dup	XM_005267523.1:c.-8-547_-8-541dup	XM_005267523.1:c.-8-548_-8-541dup	XM_005267523.1:c.-8-549_-8-541dup	XM_005267523.1:c.-8-550_-8-541dup	XM_005267523.1:c.-8-551_-8-541dup	XM_005267523.1:c.-8-552_-8-541dup	XM_005267523.1:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005267523.1:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant X4	XM_005267525.1:c.-42-560=	XM_005267525.1:c.-42-551_-42-541del	XM_005267525.1:c.-42-550_-42-541del	XM_005267525.1:c.-42-548_-42-541del	XM_005267525.1:c.-42-547_-42-541del	XM_005267525.1:c.-42-545_-42-541del	XM_005267525.1:c.-42-544_-42-541del	XM_005267525.1:c.-42-543_-42-541del	XM_005267525.1:c.-42-542_-42-541del	XM_005267525.1:c.-42-541del	XM_005267525.1:c.-42-541dup	XM_005267525.1:c.-42-542_-42-541dup	XM_005267525.1:c.-42-543_-42-541dup	XM_005267525.1:c.-42-544_-42-541dup	XM_005267525.1:c.-42-545_-42-541dup	XM_005267525.1:c.-42-546_-42-541dup	XM_005267525.1:c.-42-547_-42-541dup	XM_005267525.1:c.-42-548_-42-541dup	XM_005267525.1:c.-42-549_-42-541dup	XM_005267525.1:c.-42-550_-42-541dup	XM_005267525.1:c.-42-551_-42-541dup	XM_005267525.1:c.-42-552_-42-541dup	XM_005267525.1:c.-42-541_-42-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005267525.1:c.-42-541_-42-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant X5	XM_005267526.1:c.-42-560=	XM_005267526.1:c.-42-551_-42-541del	XM_005267526.1:c.-42-550_-42-541del	XM_005267526.1:c.-42-548_-42-541del	XM_005267526.1:c.-42-547_-42-541del	XM_005267526.1:c.-42-545_-42-541del	XM_005267526.1:c.-42-544_-42-541del	XM_005267526.1:c.-42-543_-42-541del	XM_005267526.1:c.-42-542_-42-541del	XM_005267526.1:c.-42-541del	XM_005267526.1:c.-42-541dup	XM_005267526.1:c.-42-542_-42-541dup	XM_005267526.1:c.-42-543_-42-541dup	XM_005267526.1:c.-42-544_-42-541dup	XM_005267526.1:c.-42-545_-42-541dup	XM_005267526.1:c.-42-546_-42-541dup	XM_005267526.1:c.-42-547_-42-541dup	XM_005267526.1:c.-42-548_-42-541dup	XM_005267526.1:c.-42-549_-42-541dup	XM_005267526.1:c.-42-550_-42-541dup	XM_005267526.1:c.-42-551_-42-541dup	XM_005267526.1:c.-42-552_-42-541dup	XM_005267526.1:c.-42-541_-42-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005267526.1:c.-42-541_-42-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant X6	XM_005267527.1:c.-208-2391=	XM_005267527.1:c.-208-2382_-208-2372del	XM_005267527.1:c.-208-2381_-208-2372del	XM_005267527.1:c.-208-2379_-208-2372del	XM_005267527.1:c.-208-2378_-208-2372del	XM_005267527.1:c.-208-2376_-208-2372del	XM_005267527.1:c.-208-2375_-208-2372del	XM_005267527.1:c.-208-2374_-208-2372del	XM_005267527.1:c.-208-2373_-208-2372del	XM_005267527.1:c.-208-2372del	XM_005267527.1:c.-208-2372dup	XM_005267527.1:c.-208-2373_-208-2372dup	XM_005267527.1:c.-208-2374_-208-2372dup	XM_005267527.1:c.-208-2375_-208-2372dup	XM_005267527.1:c.-208-2376_-208-2372dup	XM_005267527.1:c.-208-2377_-208-2372dup	XM_005267527.1:c.-208-2378_-208-2372dup	XM_005267527.1:c.-208-2379_-208-2372dup	XM_005267527.1:c.-208-2380_-208-2372dup	XM_005267527.1:c.-208-2381_-208-2372dup	XM_005267527.1:c.-208-2382_-208-2372dup	XM_005267527.1:c.-208-2383_-208-2372dup	XM_005267527.1:c.-208-2372_-208-2371insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005267527.1:c.-208-2372_-208-2371insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant X7	XM_017021205.2:c.-8-560=	XM_017021205.2:c.-8-551_-8-541del	XM_017021205.2:c.-8-550_-8-541del	XM_017021205.2:c.-8-548_-8-541del	XM_017021205.2:c.-8-547_-8-541del	XM_017021205.2:c.-8-545_-8-541del	XM_017021205.2:c.-8-544_-8-541del	XM_017021205.2:c.-8-543_-8-541del	XM_017021205.2:c.-8-542_-8-541del	XM_017021205.2:c.-8-541del	XM_017021205.2:c.-8-541dup	XM_017021205.2:c.-8-542_-8-541dup	XM_017021205.2:c.-8-543_-8-541dup	XM_017021205.2:c.-8-544_-8-541dup	XM_017021205.2:c.-8-545_-8-541dup	XM_017021205.2:c.-8-546_-8-541dup	XM_017021205.2:c.-8-547_-8-541dup	XM_017021205.2:c.-8-548_-8-541dup	XM_017021205.2:c.-8-549_-8-541dup	XM_017021205.2:c.-8-550_-8-541dup	XM_017021205.2:c.-8-551_-8-541dup	XM_017021205.2:c.-8-552_-8-541dup	XM_017021205.2:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_017021205.2:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant X8	XM_017021206.2:c.-8-560=	XM_017021206.2:c.-8-551_-8-541del	XM_017021206.2:c.-8-550_-8-541del	XM_017021206.2:c.-8-548_-8-541del	XM_017021206.2:c.-8-547_-8-541del	XM_017021206.2:c.-8-545_-8-541del	XM_017021206.2:c.-8-544_-8-541del	XM_017021206.2:c.-8-543_-8-541del	XM_017021206.2:c.-8-542_-8-541del	XM_017021206.2:c.-8-541del	XM_017021206.2:c.-8-541dup	XM_017021206.2:c.-8-542_-8-541dup	XM_017021206.2:c.-8-543_-8-541dup	XM_017021206.2:c.-8-544_-8-541dup	XM_017021206.2:c.-8-545_-8-541dup	XM_017021206.2:c.-8-546_-8-541dup	XM_017021206.2:c.-8-547_-8-541dup	XM_017021206.2:c.-8-548_-8-541dup	XM_017021206.2:c.-8-549_-8-541dup	XM_017021206.2:c.-8-550_-8-541dup	XM_017021206.2:c.-8-551_-8-541dup	XM_017021206.2:c.-8-552_-8-541dup	XM_017021206.2:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_017021206.2:c.-8-541_-8-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant X10	XM_017021213.3:c.-42-560=	XM_017021213.3:c.-42-551_-42-541del	XM_017021213.3:c.-42-550_-42-541del	XM_017021213.3:c.-42-548_-42-541del	XM_017021213.3:c.-42-547_-42-541del	XM_017021213.3:c.-42-545_-42-541del	XM_017021213.3:c.-42-544_-42-541del	XM_017021213.3:c.-42-543_-42-541del	XM_017021213.3:c.-42-542_-42-541del	XM_017021213.3:c.-42-541del	XM_017021213.3:c.-42-541dup	XM_017021213.3:c.-42-542_-42-541dup	XM_017021213.3:c.-42-543_-42-541dup	XM_017021213.3:c.-42-544_-42-541dup	XM_017021213.3:c.-42-545_-42-541dup	XM_017021213.3:c.-42-546_-42-541dup	XM_017021213.3:c.-42-547_-42-541dup	XM_017021213.3:c.-42-548_-42-541dup	XM_017021213.3:c.-42-549_-42-541dup	XM_017021213.3:c.-42-550_-42-541dup	XM_017021213.3:c.-42-551_-42-541dup	XM_017021213.3:c.-42-552_-42-541dup	XM_017021213.3:c.-42-541_-42-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_017021213.3:c.-42-541_-42-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant X2	XM_047431254.1:c.65-560=	XM_047431254.1:c.65-551_65-541del	XM_047431254.1:c.65-550_65-541del	XM_047431254.1:c.65-548_65-541del	XM_047431254.1:c.65-547_65-541del	XM_047431254.1:c.65-545_65-541del	XM_047431254.1:c.65-544_65-541del	XM_047431254.1:c.65-543_65-541del	XM_047431254.1:c.65-542_65-541del	XM_047431254.1:c.65-541del	XM_047431254.1:c.65-541dup	XM_047431254.1:c.65-542_65-541dup	XM_047431254.1:c.65-543_65-541dup	XM_047431254.1:c.65-544_65-541dup	XM_047431254.1:c.65-545_65-541dup	XM_047431254.1:c.65-546_65-541dup	XM_047431254.1:c.65-547_65-541dup	XM_047431254.1:c.65-548_65-541dup	XM_047431254.1:c.65-549_65-541dup	XM_047431254.1:c.65-550_65-541dup	XM_047431254.1:c.65-551_65-541dup	XM_047431254.1:c.65-552_65-541dup	XM_047431254.1:c.65-541_65-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_047431254.1:c.65-541_65-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant X3	XM_047431255.1:c.65-560=	XM_047431255.1:c.65-551_65-541del	XM_047431255.1:c.65-550_65-541del	XM_047431255.1:c.65-548_65-541del	XM_047431255.1:c.65-547_65-541del	XM_047431255.1:c.65-545_65-541del	XM_047431255.1:c.65-544_65-541del	XM_047431255.1:c.65-543_65-541del	XM_047431255.1:c.65-542_65-541del	XM_047431255.1:c.65-541del	XM_047431255.1:c.65-541dup	XM_047431255.1:c.65-542_65-541dup	XM_047431255.1:c.65-543_65-541dup	XM_047431255.1:c.65-544_65-541dup	XM_047431255.1:c.65-545_65-541dup	XM_047431255.1:c.65-546_65-541dup	XM_047431255.1:c.65-547_65-541dup	XM_047431255.1:c.65-548_65-541dup	XM_047431255.1:c.65-549_65-541dup	XM_047431255.1:c.65-550_65-541dup	XM_047431255.1:c.65-551_65-541dup	XM_047431255.1:c.65-552_65-541dup	XM_047431255.1:c.65-541_65-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_047431255.1:c.65-541_65-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant X5	XM_047431256.1:c.65-560=	XM_047431256.1:c.65-551_65-541del	XM_047431256.1:c.65-550_65-541del	XM_047431256.1:c.65-548_65-541del	XM_047431256.1:c.65-547_65-541del	XM_047431256.1:c.65-545_65-541del	XM_047431256.1:c.65-544_65-541del	XM_047431256.1:c.65-543_65-541del	XM_047431256.1:c.65-542_65-541del	XM_047431256.1:c.65-541del	XM_047431256.1:c.65-541dup	XM_047431256.1:c.65-542_65-541dup	XM_047431256.1:c.65-543_65-541dup	XM_047431256.1:c.65-544_65-541dup	XM_047431256.1:c.65-545_65-541dup	XM_047431256.1:c.65-546_65-541dup	XM_047431256.1:c.65-547_65-541dup	XM_047431256.1:c.65-548_65-541dup	XM_047431256.1:c.65-549_65-541dup	XM_047431256.1:c.65-550_65-541dup	XM_047431256.1:c.65-551_65-541dup	XM_047431256.1:c.65-552_65-541dup	XM_047431256.1:c.65-541_65-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_047431256.1:c.65-541_65-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant X6	XM_047431257.1:c.65-560=	XM_047431257.1:c.65-551_65-541del	XM_047431257.1:c.65-550_65-541del	XM_047431257.1:c.65-548_65-541del	XM_047431257.1:c.65-547_65-541del	XM_047431257.1:c.65-545_65-541del	XM_047431257.1:c.65-544_65-541del	XM_047431257.1:c.65-543_65-541del	XM_047431257.1:c.65-542_65-541del	XM_047431257.1:c.65-541del	XM_047431257.1:c.65-541dup	XM_047431257.1:c.65-542_65-541dup	XM_047431257.1:c.65-543_65-541dup	XM_047431257.1:c.65-544_65-541dup	XM_047431257.1:c.65-545_65-541dup	XM_047431257.1:c.65-546_65-541dup	XM_047431257.1:c.65-547_65-541dup	XM_047431257.1:c.65-548_65-541dup	XM_047431257.1:c.65-549_65-541dup	XM_047431257.1:c.65-550_65-541dup	XM_047431257.1:c.65-551_65-541dup	XM_047431257.1:c.65-552_65-541dup	XM_047431257.1:c.65-541_65-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_047431257.1:c.65-541_65-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant X9	XM_047431258.1:c.-42-560=	XM_047431258.1:c.-42-551_-42-541del	XM_047431258.1:c.-42-550_-42-541del	XM_047431258.1:c.-42-548_-42-541del	XM_047431258.1:c.-42-547_-42-541del	XM_047431258.1:c.-42-545_-42-541del	XM_047431258.1:c.-42-544_-42-541del	XM_047431258.1:c.-42-543_-42-541del	XM_047431258.1:c.-42-542_-42-541del	XM_047431258.1:c.-42-541del	XM_047431258.1:c.-42-541dup	XM_047431258.1:c.-42-542_-42-541dup	XM_047431258.1:c.-42-543_-42-541dup	XM_047431258.1:c.-42-544_-42-541dup	XM_047431258.1:c.-42-545_-42-541dup	XM_047431258.1:c.-42-546_-42-541dup	XM_047431258.1:c.-42-547_-42-541dup	XM_047431258.1:c.-42-548_-42-541dup	XM_047431258.1:c.-42-549_-42-541dup	XM_047431258.1:c.-42-550_-42-541dup	XM_047431258.1:c.-42-551_-42-541dup	XM_047431258.1:c.-42-552_-42-541dup	XM_047431258.1:c.-42-541_-42-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_047431258.1:c.-42-541_-42-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant X11	XM_047431259.1:c.-42-560=	XM_047431259.1:c.-42-551_-42-541del	XM_047431259.1:c.-42-550_-42-541del	XM_047431259.1:c.-42-548_-42-541del	XM_047431259.1:c.-42-547_-42-541del	XM_047431259.1:c.-42-545_-42-541del	XM_047431259.1:c.-42-544_-42-541del	XM_047431259.1:c.-42-543_-42-541del	XM_047431259.1:c.-42-542_-42-541del	XM_047431259.1:c.-42-541del	XM_047431259.1:c.-42-541dup	XM_047431259.1:c.-42-542_-42-541dup	XM_047431259.1:c.-42-543_-42-541dup	XM_047431259.1:c.-42-544_-42-541dup	XM_047431259.1:c.-42-545_-42-541dup	XM_047431259.1:c.-42-546_-42-541dup	XM_047431259.1:c.-42-547_-42-541dup	XM_047431259.1:c.-42-548_-42-541dup	XM_047431259.1:c.-42-549_-42-541dup	XM_047431259.1:c.-42-550_-42-541dup	XM_047431259.1:c.-42-551_-42-541dup	XM_047431259.1:c.-42-552_-42-541dup	XM_047431259.1:c.-42-541_-42-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_047431259.1:c.-42-541_-42-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DCAF4 transcript variant X12	XM_047431260.1:c.-42-560=	XM_047431260.1:c.-42-551_-42-541del	XM_047431260.1:c.-42-550_-42-541del	XM_047431260.1:c.-42-548_-42-541del	XM_047431260.1:c.-42-547_-42-541del	XM_047431260.1:c.-42-545_-42-541del	XM_047431260.1:c.-42-544_-42-541del	XM_047431260.1:c.-42-543_-42-541del	XM_047431260.1:c.-42-542_-42-541del	XM_047431260.1:c.-42-541del	XM_047431260.1:c.-42-541dup	XM_047431260.1:c.-42-542_-42-541dup	XM_047431260.1:c.-42-543_-42-541dup	XM_047431260.1:c.-42-544_-42-541dup	XM_047431260.1:c.-42-545_-42-541dup	XM_047431260.1:c.-42-546_-42-541dup	XM_047431260.1:c.-42-547_-42-541dup	XM_047431260.1:c.-42-548_-42-541dup	XM_047431260.1:c.-42-549_-42-541dup	XM_047431260.1:c.-42-550_-42-541dup	XM_047431260.1:c.-42-551_-42-541dup	XM_047431260.1:c.-42-552_-42-541dup	XM_047431260.1:c.-42-541_-42-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_047431260.1:c.-42-541_-42-540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

59 SubSNP, 35 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81176750	Dec 15, 2007 (137)
2	SSIP	ss947332207	Aug 21, 2014 (142)
3	EVA_GENOME_DK	ss1574782499	Apr 01, 2015 (144)
4	SWEGEN	ss3012442469	Nov 08, 2017 (151)
5	URBANLAB	ss3650236264	Oct 12, 2018 (152)
6	EVA_DECODE	ss3696971107	Jul 13, 2019 (153)
7	EVA_DECODE	ss3696971108	Jul 13, 2019 (153)
8	EVA_DECODE	ss3696971109	Jul 13, 2019 (153)
9	EVA_DECODE	ss3696971110	Jul 13, 2019 (153)
10	EVA_DECODE	ss3696971111	Jul 13, 2019 (153)
11	PACBIO	ss3787706293	Jul 13, 2019 (153)
12	PACBIO	ss3792738001	Jul 13, 2019 (153)
13	PACBIO	ss3792738002	Jul 13, 2019 (153)
14	PACBIO	ss3797622334	Jul 13, 2019 (153)
15	PACBIO	ss3797622335	Jul 13, 2019 (153)
16	EVA	ss3833995718	Apr 27, 2020 (154)
17	GNOMAD	ss4280602290	Apr 26, 2021 (155)
18	GNOMAD	ss4280602291	Apr 26, 2021 (155)
19	GNOMAD	ss4280602292	Apr 26, 2021 (155)
20	GNOMAD	ss4280602293	Apr 26, 2021 (155)
21	GNOMAD	ss4280602294	Apr 26, 2021 (155)
22	GNOMAD	ss4280602295	Apr 26, 2021 (155)
23	GNOMAD	ss4280602296	Apr 26, 2021 (155)
24	GNOMAD	ss4280602297	Apr 26, 2021 (155)
25	GNOMAD	ss4280602298	Apr 26, 2021 (155)
26	GNOMAD	ss4280602299	Apr 26, 2021 (155)
27	GNOMAD	ss4280602300	Apr 26, 2021 (155)
28	GNOMAD	ss4280602301	Apr 26, 2021 (155)
29	GNOMAD	ss4280602302	Apr 26, 2021 (155)
30	GNOMAD	ss4280602303	Apr 26, 2021 (155)
31	GNOMAD	ss4280602304	Apr 26, 2021 (155)
32	GNOMAD	ss4280602305	Apr 26, 2021 (155)
33	GNOMAD	ss4280602306	Apr 26, 2021 (155)
34	GNOMAD	ss4280602307	Apr 26, 2021 (155)
35	GNOMAD	ss4280602308	Apr 26, 2021 (155)
36	GNOMAD	ss4280602309	Apr 26, 2021 (155)
37	GNOMAD	ss4280602310	Apr 26, 2021 (155)
38	GNOMAD	ss4280602311	Apr 26, 2021 (155)
39	TOPMED	ss4975783683	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5213898857	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5213898858	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5213898859	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5213898860	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5213898861	Apr 26, 2021 (155)
45	1000G_HIGH_COVERAGE	ss5296740682	Oct 16, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5296740683	Oct 16, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5296740684	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5490734060	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5490734061	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5490734062	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5490734063	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5766894253	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5766894254	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5766894255	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5766894257	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5766894258	Oct 16, 2022 (156)
57	EVA	ss5841314254	Oct 16, 2022 (156)
58	EVA	ss5841314255	Oct 16, 2022 (156)
59	EVA	ss5901937363	Oct 16, 2022 (156)
60	The Danish reference pan genome	NC_000014.8 - 73404119	Apr 27, 2020 (154)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455458901 (NC_000014.9:72937410::T 30248/97194) Row 455458902 (NC_000014.9:72937410::TT 21383/97142) Row 455458903 (NC_000014.9:72937410::TTT 333/97260)...	-	Apr 26, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 71868164 (NC_000014.8:73404118::TT 1238/15716) Row 71868165 (NC_000014.8:73404118::T 6461/15716) Row 71868166 (NC_000014.8:73404118:T: 1493/15716)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 71868164 (NC_000014.8:73404118::TT 1238/15716) Row 71868165 (NC_000014.8:73404118::T 6461/15716) Row 71868166 (NC_000014.8:73404118:T: 1493/15716)...	-	Apr 26, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 71868164 (NC_000014.8:73404118::TT 1238/15716) Row 71868165 (NC_000014.8:73404118::T 6461/15716) Row 71868166 (NC_000014.8:73404118:T: 1493/15716)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 71868164 (NC_000014.8:73404118::TT 1238/15716) Row 71868165 (NC_000014.8:73404118::T 6461/15716) Row 71868166 (NC_000014.8:73404118:T: 1493/15716)...	-	Apr 26, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 71868164 (NC_000014.8:73404118::TT 1238/15716) Row 71868165 (NC_000014.8:73404118::T 6461/15716) Row 71868166 (NC_000014.8:73404118:T: 1493/15716)...	-	Apr 26, 2021 (155)
88	14KJPN Submission ignored due to conflicting rows: Row 100731357 (NC_000014.9:72937410::TT 2135/26746) Row 100731358 (NC_000014.9:72937410::T 11559/26746) Row 100731359 (NC_000014.9:72937410:T: 2796/26746)...	-	Oct 16, 2022 (156)
89	14KJPN Submission ignored due to conflicting rows: Row 100731357 (NC_000014.9:72937410::TT 2135/26746) Row 100731358 (NC_000014.9:72937410::T 11559/26746) Row 100731359 (NC_000014.9:72937410:T: 2796/26746)...	-	Oct 16, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 100731357 (NC_000014.9:72937410::TT 2135/26746) Row 100731358 (NC_000014.9:72937410::T 11559/26746) Row 100731359 (NC_000014.9:72937410:T: 2796/26746)...	-	Oct 16, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 100731357 (NC_000014.9:72937410::TT 2135/26746) Row 100731358 (NC_000014.9:72937410::T 11559/26746) Row 100731359 (NC_000014.9:72937410:T: 2796/26746)...	-	Oct 16, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 100731357 (NC_000014.9:72937410::TT 2135/26746) Row 100731358 (NC_000014.9:72937410::T 11559/26746) Row 100731359 (NC_000014.9:72937410:T: 2796/26746)...	-	Oct 16, 2022 (156)
93	TopMed	NC_000014.9 - 72937411	Apr 26, 2021 (155)
94	ALFA	NC_000014.9 - 72937411	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs34526241	May 11, 2012 (137)
rs59866072	May 11, 2012 (137)
rs72179393	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
889919757	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4280602311	NC_000014.9:72937410:TTTTTTTTTT:	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
889919757	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
191329342, ss4280602310, ss4975783683	NC_000014.9:72937410:TTTTTTTT:	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
889919757	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4280602309	NC_000014.9:72937410:TTTTTTT:	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
889919757	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4280602308	NC_000014.9:72937410:TTTTT:	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4280602307	NC_000014.9:72937410:TTTT:	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
889919757	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4280602306	NC_000014.9:72937410:TTT:	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
889919757	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4280602305	NC_000014.9:72937410:TT:	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
889919757	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss81176750	NC_000014.7:72473890:T:	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3012442469, ss5213898859	NC_000014.8:73404118:T:	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3696971107, ss4280602304, ss5296740683, ss5490734062, ss5766894255	NC_000014.9:72937410:T:	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
889919757	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss947332207, ss3787706293, ss3792738001, ss3797622334, ss3833995718, ss5213898858	NC_000014.8:73404118::T	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3650236264, ss4280602290, ss5296740682, ss5490734061, ss5766894254	NC_000014.9:72937410::T	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
889919757	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3696971108	NC_000014.9:72937411::T	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
460116, ss1574782499, ss3792738002, ss3797622335, ss5213898857, ss5841314254	NC_000014.8:73404118::TT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280602291, ss5296740684, ss5490734060, ss5766894253, ss5901937363	NC_000014.9:72937410::TT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
889919757	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3696971109	NC_000014.9:72937411::TT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5213898861, ss5841314255	NC_000014.8:73404118::TTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280602292, ss5490734063, ss5766894258	NC_000014.9:72937410::TTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
889919757	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3696971110	NC_000014.9:72937411::TTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280602293	NC_000014.9:72937410::TTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
889919757	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280602294	NC_000014.9:72937410::TTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5213898860	NC_000014.8:73404118::TTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280602295, ss5766894257	NC_000014.9:72937410::TTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
889919757	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3696971111	NC_000014.9:72937411::TTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280602296	NC_000014.9:72937410::TTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
889919757	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280602297	NC_000014.9:72937410::TTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280602298	NC_000014.9:72937410::TTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280602299	NC_000014.9:72937410::TTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280602300	NC_000014.9:72937410::TTTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280602301	NC_000014.9:72937410::TTTTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280602302	NC_000014.9:72937410::TTTTTTTTTTTT… NC_000014.9:72937410::TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280602303	NC_000014.9:72937410::TTTTTTTTTTTT… NC_000014.9:72937410::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:72937410:TTTTTTTTTTTTT… NC_000014.9:72937410:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs11288108

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs11288108