Name: rs112648110
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.

rs112648110

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:32195978-32195992 (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)₈ / del(T)₇ / del(T)₆ / del(…
del(T)₈ / del(T)₇ / del(T)₆ / 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)₁₃ / dup(T)₁₄ / dup(T)₁₅ / ins(T)₁₆ / ins(T)₁₇ / ins(T)₁₈ / ins(T)₁₉ / ins(T)₂₀
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.02733 (370/13538, ALFA)
(T)₁₅=0.05 (2/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TXLNA : 3 Prime UTR Variant
CCDC28B : 2KB Upstream 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	13538	TTTTTTTTTTTTTTT=0.96580	TTTTTTT=0.00000, TTTTTTTT=0.00000, TTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.02733, TTTTTTTTTTTTTTTT=0.00044, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00140, TTTTTTTTTTTTTTTTTTTTT=0.00340, TTTTTTTTTTTTTTTTTTTTTTTT=0.00066, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00096	0.94699	0.001797	0.051213	6
European	Sub	11108	TTTTTTTTTTTTTTT=0.95832	TTTTTTT=0.00000, TTTTTTTT=0.00000, TTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.03331, TTTTTTTTTTTTTTTT=0.00054, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00171, TTTTTTTTTTTTTTTTTTTTT=0.00414, TTTTTTTTTTTTTTTTTTTTTTTT=0.00081, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00117	0.9352	0.002197	0.062603	4
African	Sub	1468	TTTTTTTTTTTTTTT=1.0000	TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	52	TTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1416	TTTTTTTTTTTTTTT=1.0000	TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	52	TTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	38	TTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	14	TTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	102	TTTTTTTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	436	TTTTTTTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	54	TTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	318	TTTTTTTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A

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
Allele Frequency Aggregator	Total	Global	13538	(T)₁₅=0.96580	del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.02733, dupT=0.00044, dupTT=0.00000, dupTTT=0.00000, dup(T)₄=0.00140, dup(T)₆=0.00340, dup(T)₉=0.00066, ins(T)₂₀=0.00096
Allele Frequency Aggregator	European	Sub	11108	(T)₁₅=0.95832	del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.03331, dupT=0.00054, dupTT=0.00000, dupTTT=0.00000, dup(T)₄=0.00171, dup(T)₆=0.00414, dup(T)₉=0.00081, ins(T)₂₀=0.00117
Allele Frequency Aggregator	African	Sub	1468	(T)₁₅=1.0000	del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₆=0.0000, dup(T)₉=0.0000, ins(T)₂₀=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	436	(T)₁₅=1.000	del(T)₈=0.000, del(T)₇=0.000, del(T)₆=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)₉=0.000, ins(T)₂₀=0.000
Allele Frequency Aggregator	Other	Sub	318	(T)₁₅=1.000	del(T)₈=0.000, del(T)₇=0.000, del(T)₆=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)₉=0.000, ins(T)₂₀=0.000
Allele Frequency Aggregator	Latin American 1	Sub	102	(T)₁₅=1.000	del(T)₈=0.000, del(T)₇=0.000, del(T)₆=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)₉=0.000, ins(T)₂₀=0.000
Allele Frequency Aggregator	South Asian	Sub	54	(T)₁₅=1.00	del(T)₈=0.00, del(T)₇=0.00, del(T)₆=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)₉=0.00, ins(T)₂₀=0.00
Allele Frequency Aggregator	Asian	Sub	52	(T)₁₅=1.00	del(T)₈=0.00, del(T)₇=0.00, del(T)₆=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)₉=0.00, ins(T)₂₀=0.00
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dup(T)₁₃=0.95

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 1	NC_000001.11:g.32195985_32195992del
GRCh38.p14 chr 1	NC_000001.11:g.32195986_32195992del
GRCh38.p14 chr 1	NC_000001.11:g.32195987_32195992del
GRCh38.p14 chr 1	NC_000001.11:g.32195989_32195992del
GRCh38.p14 chr 1	NC_000001.11:g.32195990_32195992del
GRCh38.p14 chr 1	NC_000001.11:g.32195991_32195992del
GRCh38.p14 chr 1	NC_000001.11:g.32195992del
GRCh38.p14 chr 1	NC_000001.11:g.32195992dup
GRCh38.p14 chr 1	NC_000001.11:g.32195991_32195992dup
GRCh38.p14 chr 1	NC_000001.11:g.32195990_32195992dup
GRCh38.p14 chr 1	NC_000001.11:g.32195989_32195992dup
GRCh38.p14 chr 1	NC_000001.11:g.32195988_32195992dup
GRCh38.p14 chr 1	NC_000001.11:g.32195987_32195992dup
GRCh38.p14 chr 1	NC_000001.11:g.32195986_32195992dup
GRCh38.p14 chr 1	NC_000001.11:g.32195985_32195992dup
GRCh38.p14 chr 1	NC_000001.11:g.32195984_32195992dup
GRCh38.p14 chr 1	NC_000001.11:g.32195983_32195992dup
GRCh38.p14 chr 1	NC_000001.11:g.32195980_32195992dup
GRCh38.p14 chr 1	NC_000001.11:g.32195979_32195992dup
GRCh38.p14 chr 1	NC_000001.11:g.32195978_32195992dup
GRCh38.p14 chr 1	NC_000001.11:g.32195992_32195993insTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.32195992_32195993insTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.32195992_32195993insTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.32195992_32195993insTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.32195992_32195993insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.32661586_32661593del
GRCh37.p13 chr 1	NC_000001.10:g.32661587_32661593del
GRCh37.p13 chr 1	NC_000001.10:g.32661588_32661593del
GRCh37.p13 chr 1	NC_000001.10:g.32661590_32661593del
GRCh37.p13 chr 1	NC_000001.10:g.32661591_32661593del
GRCh37.p13 chr 1	NC_000001.10:g.32661592_32661593del
GRCh37.p13 chr 1	NC_000001.10:g.32661593del
GRCh37.p13 chr 1	NC_000001.10:g.32661593dup
GRCh37.p13 chr 1	NC_000001.10:g.32661592_32661593dup
GRCh37.p13 chr 1	NC_000001.10:g.32661591_32661593dup
GRCh37.p13 chr 1	NC_000001.10:g.32661590_32661593dup
GRCh37.p13 chr 1	NC_000001.10:g.32661589_32661593dup
GRCh37.p13 chr 1	NC_000001.10:g.32661588_32661593dup
GRCh37.p13 chr 1	NC_000001.10:g.32661587_32661593dup
GRCh37.p13 chr 1	NC_000001.10:g.32661586_32661593dup
GRCh37.p13 chr 1	NC_000001.10:g.32661585_32661593dup
GRCh37.p13 chr 1	NC_000001.10:g.32661584_32661593dup
GRCh37.p13 chr 1	NC_000001.10:g.32661581_32661593dup
GRCh37.p13 chr 1	NC_000001.10:g.32661580_32661593dup
GRCh37.p13 chr 1	NC_000001.10:g.32661579_32661593dup
GRCh37.p13 chr 1	NC_000001.10:g.32661593_32661594insTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.32661593_32661594insTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.32661593_32661594insTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.32661593_32661594insTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.32661593_32661594insTTTTTTTTTTTTTTTTTTTT
CCDC28B RefSeqGene	NG_012178.1:g.385_392del
CCDC28B RefSeqGene	NG_012178.1:g.386_392del
CCDC28B RefSeqGene	NG_012178.1:g.387_392del
CCDC28B RefSeqGene	NG_012178.1:g.389_392del
CCDC28B RefSeqGene	NG_012178.1:g.390_392del
CCDC28B RefSeqGene	NG_012178.1:g.391_392del
CCDC28B RefSeqGene	NG_012178.1:g.392del
CCDC28B RefSeqGene	NG_012178.1:g.392dup
CCDC28B RefSeqGene	NG_012178.1:g.391_392dup
CCDC28B RefSeqGene	NG_012178.1:g.390_392dup
CCDC28B RefSeqGene	NG_012178.1:g.389_392dup
CCDC28B RefSeqGene	NG_012178.1:g.388_392dup
CCDC28B RefSeqGene	NG_012178.1:g.387_392dup
CCDC28B RefSeqGene	NG_012178.1:g.386_392dup
CCDC28B RefSeqGene	NG_012178.1:g.385_392dup
CCDC28B RefSeqGene	NG_012178.1:g.384_392dup
CCDC28B RefSeqGene	NG_012178.1:g.383_392dup
CCDC28B RefSeqGene	NG_012178.1:g.380_392dup
CCDC28B RefSeqGene	NG_012178.1:g.379_392dup
CCDC28B RefSeqGene	NG_012178.1:g.378_392dup
CCDC28B RefSeqGene	NG_012178.1:g.392_393insTTTTTTTTTTTTTTTT
CCDC28B RefSeqGene	NG_012178.1:g.392_393insTTTTTTTTTTTTTTTTT
CCDC28B RefSeqGene	NG_012178.1:g.392_393insTTTTTTTTTTTTTTTTTT
CCDC28B RefSeqGene	NG_012178.1:g.392_393insTTTTTTTTTTTTTTTTTTT
CCDC28B RefSeqGene	NG_012178.1:g.392_393insTTTTTTTTTTTTTTTTTTTT

Gene: TXLNA, taxilin alpha (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TXLNA transcript variant 1	NM_175852.4:c.783_797=	N/A	3 Prime UTR Variant
TXLNA transcript variant 4	NM_001376859.1:c.783_79… NM_001376859.1:c.783_797=	N/A	3 Prime UTR Variant
TXLNA transcript variant 3	NM_001376858.1:c.783_79… NM_001376858.1:c.783_797=	N/A	3 Prime UTR Variant
TXLNA transcript variant 2	NM_001376857.1:c.783_79… NM_001376857.1:c.783_797=	N/A	3 Prime UTR Variant
TXLNA transcript variant X1	XM_017000561.2:c.783_79… XM_017000561.2:c.783_797=	N/A	3 Prime UTR Variant
TXLNA transcript variant X2	XM_017000563.2:c.783_79… XM_017000563.2:c.783_797=	N/A	3 Prime UTR Variant
TXLNA transcript variant X3	XM_011540932.3:c.783_79… XM_011540932.3:c.783_797=	N/A	3 Prime UTR Variant

Gene: CCDC28B, coiled-coil domain containing 28B (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
CCDC28B transcript variant 1	NM_001301011.2:c.	N/A	N/A
CCDC28B transcript variant 2	NM_024296.5:c.	N/A	N/A
CCDC28B transcript variant X1	XM_047430215.1:c.	N/A	Upstream Transcript Variant
CCDC28B transcript variant X3	XM_047430217.1:c.	N/A	Upstream Transcript Variant
CCDC28B transcript variant X2	XM_011542113.4:c.	N/A	N/A
CCDC28B transcript variant X4	XM_017002307.2:c.	N/A	N/A
CCDC28B transcript variant X5	XM_017002308.3:c.	N/A	N/A

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)₁₅=	del(T)₈	del(T)₇	del(T)₆	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)₁₃	dup(T)₁₄	dup(T)₁₅	ins(T)₁₆	ins(T)₁₇	ins(T)₁₈	ins(T)₁₉	ins(T)₂₀
GRCh38.p14 chr 1	NC_000001.11:g.32195978_32195992=	NC_000001.11:g.32195985_32195992del	NC_000001.11:g.32195986_32195992del	NC_000001.11:g.32195987_32195992del	NC_000001.11:g.32195989_32195992del	NC_000001.11:g.32195990_32195992del	NC_000001.11:g.32195991_32195992del	NC_000001.11:g.32195992del	NC_000001.11:g.32195992dup	NC_000001.11:g.32195991_32195992dup	NC_000001.11:g.32195990_32195992dup	NC_000001.11:g.32195989_32195992dup	NC_000001.11:g.32195988_32195992dup	NC_000001.11:g.32195987_32195992dup	NC_000001.11:g.32195986_32195992dup	NC_000001.11:g.32195985_32195992dup	NC_000001.11:g.32195984_32195992dup	NC_000001.11:g.32195983_32195992dup	NC_000001.11:g.32195980_32195992dup	NC_000001.11:g.32195979_32195992dup	NC_000001.11:g.32195978_32195992dup	NC_000001.11:g.32195992_32195993insTTTTTTTTTTTTTTTT	NC_000001.11:g.32195992_32195993insTTTTTTTTTTTTTTTTT	NC_000001.11:g.32195992_32195993insTTTTTTTTTTTTTTTTTT	NC_000001.11:g.32195992_32195993insTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.32195992_32195993insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.32661579_32661593=	NC_000001.10:g.32661586_32661593del	NC_000001.10:g.32661587_32661593del	NC_000001.10:g.32661588_32661593del	NC_000001.10:g.32661590_32661593del	NC_000001.10:g.32661591_32661593del	NC_000001.10:g.32661592_32661593del	NC_000001.10:g.32661593del	NC_000001.10:g.32661593dup	NC_000001.10:g.32661592_32661593dup	NC_000001.10:g.32661591_32661593dup	NC_000001.10:g.32661590_32661593dup	NC_000001.10:g.32661589_32661593dup	NC_000001.10:g.32661588_32661593dup	NC_000001.10:g.32661587_32661593dup	NC_000001.10:g.32661586_32661593dup	NC_000001.10:g.32661585_32661593dup	NC_000001.10:g.32661584_32661593dup	NC_000001.10:g.32661581_32661593dup	NC_000001.10:g.32661580_32661593dup	NC_000001.10:g.32661579_32661593dup	NC_000001.10:g.32661593_32661594insTTTTTTTTTTTTTTTT	NC_000001.10:g.32661593_32661594insTTTTTTTTTTTTTTTTT	NC_000001.10:g.32661593_32661594insTTTTTTTTTTTTTTTTTT	NC_000001.10:g.32661593_32661594insTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.32661593_32661594insTTTTTTTTTTTTTTTTTTTT
CCDC28B RefSeqGene	NG_012178.1:g.378_392=	NG_012178.1:g.385_392del	NG_012178.1:g.386_392del	NG_012178.1:g.387_392del	NG_012178.1:g.389_392del	NG_012178.1:g.390_392del	NG_012178.1:g.391_392del	NG_012178.1:g.392del	NG_012178.1:g.392dup	NG_012178.1:g.391_392dup	NG_012178.1:g.390_392dup	NG_012178.1:g.389_392dup	NG_012178.1:g.388_392dup	NG_012178.1:g.387_392dup	NG_012178.1:g.386_392dup	NG_012178.1:g.385_392dup	NG_012178.1:g.384_392dup	NG_012178.1:g.383_392dup	NG_012178.1:g.380_392dup	NG_012178.1:g.379_392dup	NG_012178.1:g.378_392dup	NG_012178.1:g.392_393insTTTTTTTTTTTTTTTT	NG_012178.1:g.392_393insTTTTTTTTTTTTTTTTT	NG_012178.1:g.392_393insTTTTTTTTTTTTTTTTTT	NG_012178.1:g.392_393insTTTTTTTTTTTTTTTTTTT	NG_012178.1:g.392_393insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant 1	NM_175852.4:c.783_797=	NM_175852.4:c.790_797del	NM_175852.4:c.791_797del	NM_175852.4:c.792_797del	NM_175852.4:c.794_797del	NM_175852.4:c.795_797del	NM_175852.4:c.796_797del	NM_175852.4:c.*797del	NM_175852.4:c.*797dup	NM_175852.4:c.796_797dup	NM_175852.4:c.795_797dup	NM_175852.4:c.794_797dup	NM_175852.4:c.793_797dup	NM_175852.4:c.792_797dup	NM_175852.4:c.791_797dup	NM_175852.4:c.790_797dup	NM_175852.4:c.789_797dup	NM_175852.4:c.788_797dup	NM_175852.4:c.785_797dup	NM_175852.4:c.784_797dup	NM_175852.4:c.783_797dup	NM_175852.4:c.797_798insTTTTTTTTTTTTTTTT	NM_175852.4:c.797_798insTTTTTTTTTTTTTTTTT	NM_175852.4:c.797_798insTTTTTTTTTTTTTTTTTT	NM_175852.4:c.797_798insTTTTTTTTTTTTTTTTTTT	NM_175852.4:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript	NM_175852.3:c.783_797=	NM_175852.3:c.790_797del	NM_175852.3:c.791_797del	NM_175852.3:c.792_797del	NM_175852.3:c.794_797del	NM_175852.3:c.795_797del	NM_175852.3:c.796_797del	NM_175852.3:c.*797del	NM_175852.3:c.*797dup	NM_175852.3:c.796_797dup	NM_175852.3:c.795_797dup	NM_175852.3:c.794_797dup	NM_175852.3:c.793_797dup	NM_175852.3:c.792_797dup	NM_175852.3:c.791_797dup	NM_175852.3:c.790_797dup	NM_175852.3:c.789_797dup	NM_175852.3:c.788_797dup	NM_175852.3:c.785_797dup	NM_175852.3:c.784_797dup	NM_175852.3:c.783_797dup	NM_175852.3:c.797_798insTTTTTTTTTTTTTTTT	NM_175852.3:c.797_798insTTTTTTTTTTTTTTTTT	NM_175852.3:c.797_798insTTTTTTTTTTTTTTTTTT	NM_175852.3:c.797_798insTTTTTTTTTTTTTTTTTTT	NM_175852.3:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant X3	XM_011540932.3:c.783_797=	XM_011540932.3:c.790_797del	XM_011540932.3:c.791_797del	XM_011540932.3:c.792_797del	XM_011540932.3:c.794_797del	XM_011540932.3:c.795_797del	XM_011540932.3:c.796_797del	XM_011540932.3:c.*797del	XM_011540932.3:c.*797dup	XM_011540932.3:c.796_797dup	XM_011540932.3:c.795_797dup	XM_011540932.3:c.794_797dup	XM_011540932.3:c.793_797dup	XM_011540932.3:c.792_797dup	XM_011540932.3:c.791_797dup	XM_011540932.3:c.790_797dup	XM_011540932.3:c.789_797dup	XM_011540932.3:c.788_797dup	XM_011540932.3:c.785_797dup	XM_011540932.3:c.784_797dup	XM_011540932.3:c.783_797dup	XM_011540932.3:c.797_798insTTTTTTTTTTTTTTTT	XM_011540932.3:c.797_798insTTTTTTTTTTTTTTTTT	XM_011540932.3:c.797_798insTTTTTTTTTTTTTTTTTT	XM_011540932.3:c.797_798insTTTTTTTTTTTTTTTTTTT	XM_011540932.3:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant X5	XM_011540932.2:c.783_797=	XM_011540932.2:c.790_797del	XM_011540932.2:c.791_797del	XM_011540932.2:c.792_797del	XM_011540932.2:c.794_797del	XM_011540932.2:c.795_797del	XM_011540932.2:c.796_797del	XM_011540932.2:c.*797del	XM_011540932.2:c.*797dup	XM_011540932.2:c.796_797dup	XM_011540932.2:c.795_797dup	XM_011540932.2:c.794_797dup	XM_011540932.2:c.793_797dup	XM_011540932.2:c.792_797dup	XM_011540932.2:c.791_797dup	XM_011540932.2:c.790_797dup	XM_011540932.2:c.789_797dup	XM_011540932.2:c.788_797dup	XM_011540932.2:c.785_797dup	XM_011540932.2:c.784_797dup	XM_011540932.2:c.783_797dup	XM_011540932.2:c.797_798insTTTTTTTTTTTTTTTT	XM_011540932.2:c.797_798insTTTTTTTTTTTTTTTTT	XM_011540932.2:c.797_798insTTTTTTTTTTTTTTTTTT	XM_011540932.2:c.797_798insTTTTTTTTTTTTTTTTTTT	XM_011540932.2:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant X3	XM_011540932.1:c.783_797=	XM_011540932.1:c.790_797del	XM_011540932.1:c.791_797del	XM_011540932.1:c.792_797del	XM_011540932.1:c.794_797del	XM_011540932.1:c.795_797del	XM_011540932.1:c.796_797del	XM_011540932.1:c.*797del	XM_011540932.1:c.*797dup	XM_011540932.1:c.796_797dup	XM_011540932.1:c.795_797dup	XM_011540932.1:c.794_797dup	XM_011540932.1:c.793_797dup	XM_011540932.1:c.792_797dup	XM_011540932.1:c.791_797dup	XM_011540932.1:c.790_797dup	XM_011540932.1:c.789_797dup	XM_011540932.1:c.788_797dup	XM_011540932.1:c.785_797dup	XM_011540932.1:c.784_797dup	XM_011540932.1:c.783_797dup	XM_011540932.1:c.797_798insTTTTTTTTTTTTTTTT	XM_011540932.1:c.797_798insTTTTTTTTTTTTTTTTT	XM_011540932.1:c.797_798insTTTTTTTTTTTTTTTTTT	XM_011540932.1:c.797_798insTTTTTTTTTTTTTTTTTTT	XM_011540932.1:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant X1	XM_017000561.2:c.783_797=	XM_017000561.2:c.790_797del	XM_017000561.2:c.791_797del	XM_017000561.2:c.792_797del	XM_017000561.2:c.794_797del	XM_017000561.2:c.795_797del	XM_017000561.2:c.796_797del	XM_017000561.2:c.*797del	XM_017000561.2:c.*797dup	XM_017000561.2:c.796_797dup	XM_017000561.2:c.795_797dup	XM_017000561.2:c.794_797dup	XM_017000561.2:c.793_797dup	XM_017000561.2:c.792_797dup	XM_017000561.2:c.791_797dup	XM_017000561.2:c.790_797dup	XM_017000561.2:c.789_797dup	XM_017000561.2:c.788_797dup	XM_017000561.2:c.785_797dup	XM_017000561.2:c.784_797dup	XM_017000561.2:c.783_797dup	XM_017000561.2:c.797_798insTTTTTTTTTTTTTTTT	XM_017000561.2:c.797_798insTTTTTTTTTTTTTTTTT	XM_017000561.2:c.797_798insTTTTTTTTTTTTTTTTTT	XM_017000561.2:c.797_798insTTTTTTTTTTTTTTTTTTT	XM_017000561.2:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant X1	XM_017000561.1:c.783_797=	XM_017000561.1:c.790_797del	XM_017000561.1:c.791_797del	XM_017000561.1:c.792_797del	XM_017000561.1:c.794_797del	XM_017000561.1:c.795_797del	XM_017000561.1:c.796_797del	XM_017000561.1:c.*797del	XM_017000561.1:c.*797dup	XM_017000561.1:c.796_797dup	XM_017000561.1:c.795_797dup	XM_017000561.1:c.794_797dup	XM_017000561.1:c.793_797dup	XM_017000561.1:c.792_797dup	XM_017000561.1:c.791_797dup	XM_017000561.1:c.790_797dup	XM_017000561.1:c.789_797dup	XM_017000561.1:c.788_797dup	XM_017000561.1:c.785_797dup	XM_017000561.1:c.784_797dup	XM_017000561.1:c.783_797dup	XM_017000561.1:c.797_798insTTTTTTTTTTTTTTTT	XM_017000561.1:c.797_798insTTTTTTTTTTTTTTTTT	XM_017000561.1:c.797_798insTTTTTTTTTTTTTTTTTT	XM_017000561.1:c.797_798insTTTTTTTTTTTTTTTTTTT	XM_017000561.1:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant X2	XM_017000563.2:c.783_797=	XM_017000563.2:c.790_797del	XM_017000563.2:c.791_797del	XM_017000563.2:c.792_797del	XM_017000563.2:c.794_797del	XM_017000563.2:c.795_797del	XM_017000563.2:c.796_797del	XM_017000563.2:c.*797del	XM_017000563.2:c.*797dup	XM_017000563.2:c.796_797dup	XM_017000563.2:c.795_797dup	XM_017000563.2:c.794_797dup	XM_017000563.2:c.793_797dup	XM_017000563.2:c.792_797dup	XM_017000563.2:c.791_797dup	XM_017000563.2:c.790_797dup	XM_017000563.2:c.789_797dup	XM_017000563.2:c.788_797dup	XM_017000563.2:c.785_797dup	XM_017000563.2:c.784_797dup	XM_017000563.2:c.783_797dup	XM_017000563.2:c.797_798insTTTTTTTTTTTTTTTT	XM_017000563.2:c.797_798insTTTTTTTTTTTTTTTTT	XM_017000563.2:c.797_798insTTTTTTTTTTTTTTTTTT	XM_017000563.2:c.797_798insTTTTTTTTTTTTTTTTTTT	XM_017000563.2:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant X3	XM_017000563.1:c.783_797=	XM_017000563.1:c.790_797del	XM_017000563.1:c.791_797del	XM_017000563.1:c.792_797del	XM_017000563.1:c.794_797del	XM_017000563.1:c.795_797del	XM_017000563.1:c.796_797del	XM_017000563.1:c.*797del	XM_017000563.1:c.*797dup	XM_017000563.1:c.796_797dup	XM_017000563.1:c.795_797dup	XM_017000563.1:c.794_797dup	XM_017000563.1:c.793_797dup	XM_017000563.1:c.792_797dup	XM_017000563.1:c.791_797dup	XM_017000563.1:c.790_797dup	XM_017000563.1:c.789_797dup	XM_017000563.1:c.788_797dup	XM_017000563.1:c.785_797dup	XM_017000563.1:c.784_797dup	XM_017000563.1:c.783_797dup	XM_017000563.1:c.797_798insTTTTTTTTTTTTTTTT	XM_017000563.1:c.797_798insTTTTTTTTTTTTTTTTT	XM_017000563.1:c.797_798insTTTTTTTTTTTTTTTTTT	XM_017000563.1:c.797_798insTTTTTTTTTTTTTTTTTTT	XM_017000563.1:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant 2	NM_001376857.1:c.783_797=	NM_001376857.1:c.790_797del	NM_001376857.1:c.791_797del	NM_001376857.1:c.792_797del	NM_001376857.1:c.794_797del	NM_001376857.1:c.795_797del	NM_001376857.1:c.796_797del	NM_001376857.1:c.*797del	NM_001376857.1:c.*797dup	NM_001376857.1:c.796_797dup	NM_001376857.1:c.795_797dup	NM_001376857.1:c.794_797dup	NM_001376857.1:c.793_797dup	NM_001376857.1:c.792_797dup	NM_001376857.1:c.791_797dup	NM_001376857.1:c.790_797dup	NM_001376857.1:c.789_797dup	NM_001376857.1:c.788_797dup	NM_001376857.1:c.785_797dup	NM_001376857.1:c.784_797dup	NM_001376857.1:c.783_797dup	NM_001376857.1:c.797_798insTTTTTTTTTTTTTTTT	NM_001376857.1:c.797_798insTTTTTTTTTTTTTTTTT	NM_001376857.1:c.797_798insTTTTTTTTTTTTTTTTTT	NM_001376857.1:c.797_798insTTTTTTTTTTTTTTTTTTT	NM_001376857.1:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant 3	NM_001376858.1:c.783_797=	NM_001376858.1:c.790_797del	NM_001376858.1:c.791_797del	NM_001376858.1:c.792_797del	NM_001376858.1:c.794_797del	NM_001376858.1:c.795_797del	NM_001376858.1:c.796_797del	NM_001376858.1:c.*797del	NM_001376858.1:c.*797dup	NM_001376858.1:c.796_797dup	NM_001376858.1:c.795_797dup	NM_001376858.1:c.794_797dup	NM_001376858.1:c.793_797dup	NM_001376858.1:c.792_797dup	NM_001376858.1:c.791_797dup	NM_001376858.1:c.790_797dup	NM_001376858.1:c.789_797dup	NM_001376858.1:c.788_797dup	NM_001376858.1:c.785_797dup	NM_001376858.1:c.784_797dup	NM_001376858.1:c.783_797dup	NM_001376858.1:c.797_798insTTTTTTTTTTTTTTTT	NM_001376858.1:c.797_798insTTTTTTTTTTTTTTTTT	NM_001376858.1:c.797_798insTTTTTTTTTTTTTTTTTT	NM_001376858.1:c.797_798insTTTTTTTTTTTTTTTTTTT	NM_001376858.1:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant 4	NM_001376859.1:c.783_797=	NM_001376859.1:c.790_797del	NM_001376859.1:c.791_797del	NM_001376859.1:c.792_797del	NM_001376859.1:c.794_797del	NM_001376859.1:c.795_797del	NM_001376859.1:c.796_797del	NM_001376859.1:c.*797del	NM_001376859.1:c.*797dup	NM_001376859.1:c.796_797dup	NM_001376859.1:c.795_797dup	NM_001376859.1:c.794_797dup	NM_001376859.1:c.793_797dup	NM_001376859.1:c.792_797dup	NM_001376859.1:c.791_797dup	NM_001376859.1:c.790_797dup	NM_001376859.1:c.789_797dup	NM_001376859.1:c.788_797dup	NM_001376859.1:c.785_797dup	NM_001376859.1:c.784_797dup	NM_001376859.1:c.783_797dup	NM_001376859.1:c.797_798insTTTTTTTTTTTTTTTT	NM_001376859.1:c.797_798insTTTTTTTTTTTTTTTTT	NM_001376859.1:c.797_798insTTTTTTTTTTTTTTTTTT	NM_001376859.1:c.797_798insTTTTTTTTTTTTTTTTTTT	NM_001376859.1:c.797_798insTTTTTTTTTTTTTTTTTTTT

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#.

61 SubSNP, 41 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BUSHMAN	ss193095488	Jul 04, 2010 (132)
2	GMI	ss287965467	May 04, 2012 (137)
3	EVA_GENOME_DK	ss1583560956	Apr 01, 2015 (144)
4	HAMMER_LAB	ss1794142121	Sep 08, 2015 (146)
5	HAMMER_LAB	ss1794142123	Jan 10, 2018 (151)
6	SWEGEN	ss2986568014	Nov 08, 2017 (151)
7	EVA_DECODE	ss3686470691	Jul 12, 2019 (153)
8	EVA_DECODE	ss3686470692	Jul 12, 2019 (153)
9	EVA_DECODE	ss3686470693	Jul 12, 2019 (153)
10	EVA_DECODE	ss3686470694	Jul 12, 2019 (153)
11	ACPOP	ss3726919428	Jul 12, 2019 (153)
12	ACPOP	ss3726919429	Jul 12, 2019 (153)
13	ACPOP	ss3726919430	Jul 12, 2019 (153)
14	EVA	ss3826100803	Apr 25, 2020 (154)
15	EVA	ss3836438393	Apr 25, 2020 (154)
16	EVA	ss3841843576	Apr 25, 2020 (154)
17	KOGIC	ss3944177731	Apr 25, 2020 (154)
18	KOGIC	ss3944177732	Apr 25, 2020 (154)
19	KOGIC	ss3944177733	Apr 25, 2020 (154)
20	KOGIC	ss3944177734	Apr 25, 2020 (154)
21	EVA	ss3986010032	Apr 25, 2021 (155)
22	GNOMAD	ss3990942364	Apr 25, 2021 (155)
23	GNOMAD	ss3990942365	Apr 25, 2021 (155)
24	GNOMAD	ss3990942366	Apr 25, 2021 (155)
25	GNOMAD	ss3990942367	Apr 25, 2021 (155)
26	GNOMAD	ss3990942368	Apr 25, 2021 (155)
27	GNOMAD	ss3990942369	Apr 25, 2021 (155)
28	GNOMAD	ss3990942370	Apr 25, 2021 (155)
29	GNOMAD	ss3990942371	Apr 25, 2021 (155)
30	GNOMAD	ss3990942372	Apr 25, 2021 (155)
31	GNOMAD	ss3990942373	Apr 25, 2021 (155)
32	GNOMAD	ss3990942374	Apr 25, 2021 (155)
33	GNOMAD	ss3990942375	Apr 25, 2021 (155)
34	GNOMAD	ss3990942376	Apr 25, 2021 (155)
35	GNOMAD	ss3990942377	Apr 25, 2021 (155)
36	GNOMAD	ss3990942378	Apr 25, 2021 (155)
37	GNOMAD	ss3990942379	Apr 25, 2021 (155)
38	GNOMAD	ss3990942380	Apr 25, 2021 (155)
39	GNOMAD	ss3990942381	Apr 25, 2021 (155)
40	GNOMAD	ss3990942382	Apr 25, 2021 (155)
41	GNOMAD	ss3990942383	Apr 25, 2021 (155)
42	TOPMED	ss4444274942	Apr 25, 2021 (155)
43	TOPMED	ss4444274943	Apr 25, 2021 (155)
44	TOPMED	ss4444274944	Apr 25, 2021 (155)
45	TOMMO_GENOMICS	ss5143228216	Apr 25, 2021 (155)
46	TOMMO_GENOMICS	ss5143228217	Apr 25, 2021 (155)
47	TOMMO_GENOMICS	ss5143228218	Apr 25, 2021 (155)
48	TOMMO_GENOMICS	ss5143228219	Apr 25, 2021 (155)
49	TOMMO_GENOMICS	ss5143228220	Apr 25, 2021 (155)
50	1000G_HIGH_COVERAGE	ss5241731286	Oct 13, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5241731287	Oct 13, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5241731288	Oct 13, 2022 (156)
53	HUGCELL_USP	ss5442855651	Oct 13, 2022 (156)
54	HUGCELL_USP	ss5442855652	Oct 13, 2022 (156)
55	HUGCELL_USP	ss5442855653	Oct 13, 2022 (156)
56	TOMMO_GENOMICS	ss5667769131	Oct 13, 2022 (156)
57	TOMMO_GENOMICS	ss5667769132	Oct 13, 2022 (156)
58	TOMMO_GENOMICS	ss5667769134	Oct 13, 2022 (156)
59	TOMMO_GENOMICS	ss5667769135	Oct 13, 2022 (156)
60	EVA	ss5848846927	Oct 13, 2022 (156)
61	EVA	ss5907642912	Oct 13, 2022 (156)
62	The Danish reference pan genome	NC_000001.10 - 32661579	Apr 25, 2020 (154)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871086 (NC_000001.11:32195977::T 334/123674) Row 6871087 (NC_000001.11:32195977::TT 9/123762) Row 6871088 (NC_000001.11:32195977::TTTTT 1/123768)...	-	Apr 25, 2021 (155)
83	Korean Genome Project Submission ignored due to conflicting rows: Row 555732 (NC_000001.11:32195978:T: 396/1832) Row 555733 (NC_000001.11:32195977:TT: 14/1832) Row 555734 (NC_000001.11:32195979::T 67/1832)...	-	Apr 25, 2020 (154)
84	Korean Genome Project Submission ignored due to conflicting rows: Row 555732 (NC_000001.11:32195978:T: 396/1832) Row 555733 (NC_000001.11:32195977:TT: 14/1832) Row 555734 (NC_000001.11:32195979::T 67/1832)...	-	Apr 25, 2020 (154)
85	Korean Genome Project Submission ignored due to conflicting rows: Row 555732 (NC_000001.11:32195978:T: 396/1832) Row 555733 (NC_000001.11:32195977:TT: 14/1832) Row 555734 (NC_000001.11:32195979::T 67/1832)...	-	Apr 25, 2020 (154)
86	Korean Genome Project Submission ignored due to conflicting rows: Row 555732 (NC_000001.11:32195978:T: 396/1832) Row 555733 (NC_000001.11:32195977:TT: 14/1832) Row 555734 (NC_000001.11:32195979::T 67/1832)...	-	Apr 25, 2020 (154)
87	Northern Sweden Submission ignored due to conflicting rows: Row 204293 (NC_000001.10:32661578::TTTTTT 14/600) Row 204294 (NC_000001.10:32661578:T: 29/600) Row 204295 (NC_000001.10:32661578::TTTTTTTTTTTTTTTTTTTT 7/600)	-	Jul 12, 2019 (153)
88	Northern Sweden Submission ignored due to conflicting rows: Row 204293 (NC_000001.10:32661578::TTTTTT 14/600) Row 204294 (NC_000001.10:32661578:T: 29/600) Row 204295 (NC_000001.10:32661578::TTTTTTTTTTTTTTTTTTTT 7/600)	-	Jul 12, 2019 (153)
89	Northern Sweden Submission ignored due to conflicting rows: Row 204293 (NC_000001.10:32661578::TTTTTT 14/600) Row 204294 (NC_000001.10:32661578:T: 29/600) Row 204295 (NC_000001.10:32661578::TTTTTTTTTTTTTTTTTTTT 7/600)	-	Jul 12, 2019 (153)
90	8.3KJPN Submission ignored due to conflicting rows: Row 1197523 (NC_000001.10:32661578:T: 3063/16754) Row 1197524 (NC_000001.10:32661578::TTTTTT 13/16754) Row 1197525 (NC_000001.10:32661578::T 20/16754)...	-	Apr 25, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 1197523 (NC_000001.10:32661578:T: 3063/16754) Row 1197524 (NC_000001.10:32661578::TTTTTT 13/16754) Row 1197525 (NC_000001.10:32661578::T 20/16754)...	-	Apr 25, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 1197523 (NC_000001.10:32661578:T: 3063/16754) Row 1197524 (NC_000001.10:32661578::TTTTTT 13/16754) Row 1197525 (NC_000001.10:32661578::T 20/16754)...	-	Apr 25, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 1197523 (NC_000001.10:32661578:T: 3063/16754) Row 1197524 (NC_000001.10:32661578::TTTTTT 13/16754) Row 1197525 (NC_000001.10:32661578::T 20/16754)...	-	Apr 25, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 1197523 (NC_000001.10:32661578:T: 3063/16754) Row 1197524 (NC_000001.10:32661578::TTTTTT 13/16754) Row 1197525 (NC_000001.10:32661578::T 20/16754)...	-	Apr 25, 2021 (155)
95	14KJPN Submission ignored due to conflicting rows: Row 1606235 (NC_000001.11:32195977:T: 4036/24596) Row 1606236 (NC_000001.11:32195977::T 31/24596) Row 1606238 (NC_000001.11:32195977:TT: 6/24596)...	-	Oct 13, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 1606235 (NC_000001.11:32195977:T: 4036/24596) Row 1606236 (NC_000001.11:32195977::T 31/24596) Row 1606238 (NC_000001.11:32195977:TT: 6/24596)...	-	Oct 13, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 1606235 (NC_000001.11:32195977:T: 4036/24596) Row 1606236 (NC_000001.11:32195977::T 31/24596) Row 1606238 (NC_000001.11:32195977:TT: 6/24596)...	-	Oct 13, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 1606235 (NC_000001.11:32195977:T: 4036/24596) Row 1606236 (NC_000001.11:32195977::T 31/24596) Row 1606238 (NC_000001.11:32195977:TT: 6/24596)...	-	Oct 13, 2022 (156)
99	TopMed Submission ignored due to conflicting rows: Row 7881277 (NC_000001.11:32195977::TTT 1/264690) Row 7881278 (NC_000001.11:32195977:TTTTTT: 27/264690) Row 7881279 (NC_000001.11:32195977:TTTTTTTT: 2/264690)	-	Apr 25, 2021 (155)
100	TopMed Submission ignored due to conflicting rows: Row 7881277 (NC_000001.11:32195977::TTT 1/264690) Row 7881278 (NC_000001.11:32195977:TTTTTT: 27/264690) Row 7881279 (NC_000001.11:32195977:TTTTTTTT: 2/264690)	-	Apr 25, 2021 (155)
101	TopMed Submission ignored due to conflicting rows: Row 7881277 (NC_000001.11:32195977::TTT 1/264690) Row 7881278 (NC_000001.11:32195977:TTTTTT: 27/264690) Row 7881279 (NC_000001.11:32195977:TTTTTTTT: 2/264690)	-	Apr 25, 2021 (155)
102	ALFA	NC_000001.11 - 32195978	Apr 25, 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)
rs796174775	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3990942383, ss4444274944	NC_000001.11:32195977:TTTTTTTT:	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTT	(self)
8270948618	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTT	(self)
ss5143228220	NC_000001.10:32661578:TTTTTTT:	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTT	(self)
ss5667769135	NC_000001.11:32195977:TTTTTTT:	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTT
8270948618	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTT	(self)
ss3990942382, ss4444274943	NC_000001.11:32195977:TTTTTT:	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTT	(self)
8270948618	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss3686470691, ss3990942381	NC_000001.11:32195977:TTTT:	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
8270948618	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3990942380	NC_000001.11:32195977:TTT:	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
8270948618	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss1794142123, ss5143228219	NC_000001.10:32661578:TT:	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3944177732, ss3990942379, ss5241731287, ss5442855653, ss5667769134, ss5907642912	NC_000001.11:32195977:TT:	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
8270948618	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3686470692	NC_000001.11:32195979:TT:	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss287965467	NC_000001.9:32434165:T:	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss1794142121, ss2986568014, ss3726919429, ss3826100803, ss3836438393, ss3986010032, ss5143228216	NC_000001.10:32661578:T:	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3841843576, ss3990942378, ss5241731286, ss5442855651, ss5667769131, ss5848846927	NC_000001.11:32195977:T:	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
8270948618	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3944177731	NC_000001.11:32195978:T:	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3686470693	NC_000001.11:32195980:T:	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss193095488	NT_032977.10:31609989:T:	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss5143228218	NC_000001.10:32661578::T	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3990942364, ss5241731288, ss5442855652, ss5667769132	NC_000001.11:32195977::T	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
8270948618	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3944177733	NC_000001.11:32195979::T	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3686470694	NC_000001.11:32195981::T	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3990942365	NC_000001.11:32195977::TT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
8270948618	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4444274942	NC_000001.11:32195977::TTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
8270948618	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
8270948618	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3990942366	NC_000001.11:32195977::TTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3726919428, ss5143228217	NC_000001.10:32661578::TTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
8270948618	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3990942367	NC_000001.11:32195977::TTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3990942368	NC_000001.11:32195977::TTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
8270948618	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3990942369	NC_000001.11:32195977::TTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1762	NC_000001.10:32661578::TTTTTTTTTTT… NC_000001.10:32661578::TTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1583560956	NC_000001.10:32661579::TTTTTTTTTTT… NC_000001.10:32661579::TTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3990942370	NC_000001.11:32195977::TTTTTTTTTTT… NC_000001.11:32195977::TTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3990942371	NC_000001.11:32195977::TTTTTTTTTTT… NC_000001.11:32195977::TTTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3990942372	NC_000001.11:32195977::TTTTTTTTTTT… NC_000001.11:32195977::TTTTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3990942373	NC_000001.11:32195977::TTTTTTTTTTT… NC_000001.11:32195977::TTTTTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3990942374	NC_000001.11:32195977::TTTTTTTTTTT… NC_000001.11:32195977::TTTTTTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3990942375	NC_000001.11:32195977::TTTTTTTTTTT… NC_000001.11:32195977::TTTTTTTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3990942376	NC_000001.11:32195977::TTTTTTTTTTT… NC_000001.11:32195977::TTTTTTTTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3944177734	NC_000001.11:32195979::TTTTTTTTTTT… NC_000001.11:32195979::TTTTTTTTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3726919430	NC_000001.10:32661578::TTTTTTTTTTT… NC_000001.10:32661578::TTTTTTTTTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3990942377	NC_000001.11:32195977::TTTTTTTTTTT… NC_000001.11:32195977::TTTTTTTTTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8270948618	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:32195977:TTTTTTTTTTTT… NC_000001.11:32195977:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs112648110

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
Top▲ Help
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.

Choose placement

Placement	(T)₁₅=	del(T)₈	del(T)₇	del(T)₆	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)₁₃	dup(T)₁₄	dup(T)₁₅	ins(T)₁₆	ins(T)₁₇	ins(T)₁₈	ins(T)₁₉	ins(T)₂₀
GRCh38.p14 chr 1	NC_000001.11:g.32195978_32195992=	NC_000001.11:g.32195985_32195992del	NC_000001.11:g.32195986_32195992del	NC_000001.11:g.32195987_32195992del	NC_000001.11:g.32195989_32195992del	NC_000001.11:g.32195990_32195992del	NC_000001.11:g.32195991_32195992del	NC_000001.11:g.32195992del	NC_000001.11:g.32195992dup	NC_000001.11:g.32195991_32195992dup	NC_000001.11:g.32195990_32195992dup	NC_000001.11:g.32195989_32195992dup	NC_000001.11:g.32195988_32195992dup	NC_000001.11:g.32195987_32195992dup	NC_000001.11:g.32195986_32195992dup	NC_000001.11:g.32195985_32195992dup	NC_000001.11:g.32195984_32195992dup	NC_000001.11:g.32195983_32195992dup	NC_000001.11:g.32195980_32195992dup	NC_000001.11:g.32195979_32195992dup	NC_000001.11:g.32195978_32195992dup	NC_000001.11:g.32195992_32195993insTTTTTTTTTTTTTTTT	NC_000001.11:g.32195992_32195993insTTTTTTTTTTTTTTTTT	NC_000001.11:g.32195992_32195993insTTTTTTTTTTTTTTTTTT	NC_000001.11:g.32195992_32195993insTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.32195992_32195993insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.32661579_32661593=	NC_000001.10:g.32661586_32661593del	NC_000001.10:g.32661587_32661593del	NC_000001.10:g.32661588_32661593del	NC_000001.10:g.32661590_32661593del	NC_000001.10:g.32661591_32661593del	NC_000001.10:g.32661592_32661593del	NC_000001.10:g.32661593del	NC_000001.10:g.32661593dup	NC_000001.10:g.32661592_32661593dup	NC_000001.10:g.32661591_32661593dup	NC_000001.10:g.32661590_32661593dup	NC_000001.10:g.32661589_32661593dup	NC_000001.10:g.32661588_32661593dup	NC_000001.10:g.32661587_32661593dup	NC_000001.10:g.32661586_32661593dup	NC_000001.10:g.32661585_32661593dup	NC_000001.10:g.32661584_32661593dup	NC_000001.10:g.32661581_32661593dup	NC_000001.10:g.32661580_32661593dup	NC_000001.10:g.32661579_32661593dup	NC_000001.10:g.32661593_32661594insTTTTTTTTTTTTTTTT	NC_000001.10:g.32661593_32661594insTTTTTTTTTTTTTTTTT	NC_000001.10:g.32661593_32661594insTTTTTTTTTTTTTTTTTT	NC_000001.10:g.32661593_32661594insTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.32661593_32661594insTTTTTTTTTTTTTTTTTTTT
CCDC28B RefSeqGene	NG_012178.1:g.378_392=	NG_012178.1:g.385_392del	NG_012178.1:g.386_392del	NG_012178.1:g.387_392del	NG_012178.1:g.389_392del	NG_012178.1:g.390_392del	NG_012178.1:g.391_392del	NG_012178.1:g.392del	NG_012178.1:g.392dup	NG_012178.1:g.391_392dup	NG_012178.1:g.390_392dup	NG_012178.1:g.389_392dup	NG_012178.1:g.388_392dup	NG_012178.1:g.387_392dup	NG_012178.1:g.386_392dup	NG_012178.1:g.385_392dup	NG_012178.1:g.384_392dup	NG_012178.1:g.383_392dup	NG_012178.1:g.380_392dup	NG_012178.1:g.379_392dup	NG_012178.1:g.378_392dup	NG_012178.1:g.392_393insTTTTTTTTTTTTTTTT	NG_012178.1:g.392_393insTTTTTTTTTTTTTTTTT	NG_012178.1:g.392_393insTTTTTTTTTTTTTTTTTT	NG_012178.1:g.392_393insTTTTTTTTTTTTTTTTTTT	NG_012178.1:g.392_393insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant 1	NM_175852.4:c.783_797=	NM_175852.4:c.790_797del	NM_175852.4:c.791_797del	NM_175852.4:c.792_797del	NM_175852.4:c.794_797del	NM_175852.4:c.795_797del	NM_175852.4:c.796_797del	NM_175852.4:c.*797del	NM_175852.4:c.*797dup	NM_175852.4:c.796_797dup	NM_175852.4:c.795_797dup	NM_175852.4:c.794_797dup	NM_175852.4:c.793_797dup	NM_175852.4:c.792_797dup	NM_175852.4:c.791_797dup	NM_175852.4:c.790_797dup	NM_175852.4:c.789_797dup	NM_175852.4:c.788_797dup	NM_175852.4:c.785_797dup	NM_175852.4:c.784_797dup	NM_175852.4:c.783_797dup	NM_175852.4:c.797_798insTTTTTTTTTTTTTTTT	NM_175852.4:c.797_798insTTTTTTTTTTTTTTTTT	NM_175852.4:c.797_798insTTTTTTTTTTTTTTTTTT	NM_175852.4:c.797_798insTTTTTTTTTTTTTTTTTTT	NM_175852.4:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript	NM_175852.3:c.783_797=	NM_175852.3:c.790_797del	NM_175852.3:c.791_797del	NM_175852.3:c.792_797del	NM_175852.3:c.794_797del	NM_175852.3:c.795_797del	NM_175852.3:c.796_797del	NM_175852.3:c.*797del	NM_175852.3:c.*797dup	NM_175852.3:c.796_797dup	NM_175852.3:c.795_797dup	NM_175852.3:c.794_797dup	NM_175852.3:c.793_797dup	NM_175852.3:c.792_797dup	NM_175852.3:c.791_797dup	NM_175852.3:c.790_797dup	NM_175852.3:c.789_797dup	NM_175852.3:c.788_797dup	NM_175852.3:c.785_797dup	NM_175852.3:c.784_797dup	NM_175852.3:c.783_797dup	NM_175852.3:c.797_798insTTTTTTTTTTTTTTTT	NM_175852.3:c.797_798insTTTTTTTTTTTTTTTTT	NM_175852.3:c.797_798insTTTTTTTTTTTTTTTTTT	NM_175852.3:c.797_798insTTTTTTTTTTTTTTTTTTT	NM_175852.3:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant X3	XM_011540932.3:c.783_797=	XM_011540932.3:c.790_797del	XM_011540932.3:c.791_797del	XM_011540932.3:c.792_797del	XM_011540932.3:c.794_797del	XM_011540932.3:c.795_797del	XM_011540932.3:c.796_797del	XM_011540932.3:c.*797del	XM_011540932.3:c.*797dup	XM_011540932.3:c.796_797dup	XM_011540932.3:c.795_797dup	XM_011540932.3:c.794_797dup	XM_011540932.3:c.793_797dup	XM_011540932.3:c.792_797dup	XM_011540932.3:c.791_797dup	XM_011540932.3:c.790_797dup	XM_011540932.3:c.789_797dup	XM_011540932.3:c.788_797dup	XM_011540932.3:c.785_797dup	XM_011540932.3:c.784_797dup	XM_011540932.3:c.783_797dup	XM_011540932.3:c.797_798insTTTTTTTTTTTTTTTT	XM_011540932.3:c.797_798insTTTTTTTTTTTTTTTTT	XM_011540932.3:c.797_798insTTTTTTTTTTTTTTTTTT	XM_011540932.3:c.797_798insTTTTTTTTTTTTTTTTTTT	XM_011540932.3:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant X5	XM_011540932.2:c.783_797=	XM_011540932.2:c.790_797del	XM_011540932.2:c.791_797del	XM_011540932.2:c.792_797del	XM_011540932.2:c.794_797del	XM_011540932.2:c.795_797del	XM_011540932.2:c.796_797del	XM_011540932.2:c.*797del	XM_011540932.2:c.*797dup	XM_011540932.2:c.796_797dup	XM_011540932.2:c.795_797dup	XM_011540932.2:c.794_797dup	XM_011540932.2:c.793_797dup	XM_011540932.2:c.792_797dup	XM_011540932.2:c.791_797dup	XM_011540932.2:c.790_797dup	XM_011540932.2:c.789_797dup	XM_011540932.2:c.788_797dup	XM_011540932.2:c.785_797dup	XM_011540932.2:c.784_797dup	XM_011540932.2:c.783_797dup	XM_011540932.2:c.797_798insTTTTTTTTTTTTTTTT	XM_011540932.2:c.797_798insTTTTTTTTTTTTTTTTT	XM_011540932.2:c.797_798insTTTTTTTTTTTTTTTTTT	XM_011540932.2:c.797_798insTTTTTTTTTTTTTTTTTTT	XM_011540932.2:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant X3	XM_011540932.1:c.783_797=	XM_011540932.1:c.790_797del	XM_011540932.1:c.791_797del	XM_011540932.1:c.792_797del	XM_011540932.1:c.794_797del	XM_011540932.1:c.795_797del	XM_011540932.1:c.796_797del	XM_011540932.1:c.*797del	XM_011540932.1:c.*797dup	XM_011540932.1:c.796_797dup	XM_011540932.1:c.795_797dup	XM_011540932.1:c.794_797dup	XM_011540932.1:c.793_797dup	XM_011540932.1:c.792_797dup	XM_011540932.1:c.791_797dup	XM_011540932.1:c.790_797dup	XM_011540932.1:c.789_797dup	XM_011540932.1:c.788_797dup	XM_011540932.1:c.785_797dup	XM_011540932.1:c.784_797dup	XM_011540932.1:c.783_797dup	XM_011540932.1:c.797_798insTTTTTTTTTTTTTTTT	XM_011540932.1:c.797_798insTTTTTTTTTTTTTTTTT	XM_011540932.1:c.797_798insTTTTTTTTTTTTTTTTTT	XM_011540932.1:c.797_798insTTTTTTTTTTTTTTTTTTT	XM_011540932.1:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant X1	XM_017000561.2:c.783_797=	XM_017000561.2:c.790_797del	XM_017000561.2:c.791_797del	XM_017000561.2:c.792_797del	XM_017000561.2:c.794_797del	XM_017000561.2:c.795_797del	XM_017000561.2:c.796_797del	XM_017000561.2:c.*797del	XM_017000561.2:c.*797dup	XM_017000561.2:c.796_797dup	XM_017000561.2:c.795_797dup	XM_017000561.2:c.794_797dup	XM_017000561.2:c.793_797dup	XM_017000561.2:c.792_797dup	XM_017000561.2:c.791_797dup	XM_017000561.2:c.790_797dup	XM_017000561.2:c.789_797dup	XM_017000561.2:c.788_797dup	XM_017000561.2:c.785_797dup	XM_017000561.2:c.784_797dup	XM_017000561.2:c.783_797dup	XM_017000561.2:c.797_798insTTTTTTTTTTTTTTTT	XM_017000561.2:c.797_798insTTTTTTTTTTTTTTTTT	XM_017000561.2:c.797_798insTTTTTTTTTTTTTTTTTT	XM_017000561.2:c.797_798insTTTTTTTTTTTTTTTTTTT	XM_017000561.2:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant X1	XM_017000561.1:c.783_797=	XM_017000561.1:c.790_797del	XM_017000561.1:c.791_797del	XM_017000561.1:c.792_797del	XM_017000561.1:c.794_797del	XM_017000561.1:c.795_797del	XM_017000561.1:c.796_797del	XM_017000561.1:c.*797del	XM_017000561.1:c.*797dup	XM_017000561.1:c.796_797dup	XM_017000561.1:c.795_797dup	XM_017000561.1:c.794_797dup	XM_017000561.1:c.793_797dup	XM_017000561.1:c.792_797dup	XM_017000561.1:c.791_797dup	XM_017000561.1:c.790_797dup	XM_017000561.1:c.789_797dup	XM_017000561.1:c.788_797dup	XM_017000561.1:c.785_797dup	XM_017000561.1:c.784_797dup	XM_017000561.1:c.783_797dup	XM_017000561.1:c.797_798insTTTTTTTTTTTTTTTT	XM_017000561.1:c.797_798insTTTTTTTTTTTTTTTTT	XM_017000561.1:c.797_798insTTTTTTTTTTTTTTTTTT	XM_017000561.1:c.797_798insTTTTTTTTTTTTTTTTTTT	XM_017000561.1:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant X2	XM_017000563.2:c.783_797=	XM_017000563.2:c.790_797del	XM_017000563.2:c.791_797del	XM_017000563.2:c.792_797del	XM_017000563.2:c.794_797del	XM_017000563.2:c.795_797del	XM_017000563.2:c.796_797del	XM_017000563.2:c.*797del	XM_017000563.2:c.*797dup	XM_017000563.2:c.796_797dup	XM_017000563.2:c.795_797dup	XM_017000563.2:c.794_797dup	XM_017000563.2:c.793_797dup	XM_017000563.2:c.792_797dup	XM_017000563.2:c.791_797dup	XM_017000563.2:c.790_797dup	XM_017000563.2:c.789_797dup	XM_017000563.2:c.788_797dup	XM_017000563.2:c.785_797dup	XM_017000563.2:c.784_797dup	XM_017000563.2:c.783_797dup	XM_017000563.2:c.797_798insTTTTTTTTTTTTTTTT	XM_017000563.2:c.797_798insTTTTTTTTTTTTTTTTT	XM_017000563.2:c.797_798insTTTTTTTTTTTTTTTTTT	XM_017000563.2:c.797_798insTTTTTTTTTTTTTTTTTTT	XM_017000563.2:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant X3	XM_017000563.1:c.783_797=	XM_017000563.1:c.790_797del	XM_017000563.1:c.791_797del	XM_017000563.1:c.792_797del	XM_017000563.1:c.794_797del	XM_017000563.1:c.795_797del	XM_017000563.1:c.796_797del	XM_017000563.1:c.*797del	XM_017000563.1:c.*797dup	XM_017000563.1:c.796_797dup	XM_017000563.1:c.795_797dup	XM_017000563.1:c.794_797dup	XM_017000563.1:c.793_797dup	XM_017000563.1:c.792_797dup	XM_017000563.1:c.791_797dup	XM_017000563.1:c.790_797dup	XM_017000563.1:c.789_797dup	XM_017000563.1:c.788_797dup	XM_017000563.1:c.785_797dup	XM_017000563.1:c.784_797dup	XM_017000563.1:c.783_797dup	XM_017000563.1:c.797_798insTTTTTTTTTTTTTTTT	XM_017000563.1:c.797_798insTTTTTTTTTTTTTTTTT	XM_017000563.1:c.797_798insTTTTTTTTTTTTTTTTTT	XM_017000563.1:c.797_798insTTTTTTTTTTTTTTTTTTT	XM_017000563.1:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant 2	NM_001376857.1:c.783_797=	NM_001376857.1:c.790_797del	NM_001376857.1:c.791_797del	NM_001376857.1:c.792_797del	NM_001376857.1:c.794_797del	NM_001376857.1:c.795_797del	NM_001376857.1:c.796_797del	NM_001376857.1:c.*797del	NM_001376857.1:c.*797dup	NM_001376857.1:c.796_797dup	NM_001376857.1:c.795_797dup	NM_001376857.1:c.794_797dup	NM_001376857.1:c.793_797dup	NM_001376857.1:c.792_797dup	NM_001376857.1:c.791_797dup	NM_001376857.1:c.790_797dup	NM_001376857.1:c.789_797dup	NM_001376857.1:c.788_797dup	NM_001376857.1:c.785_797dup	NM_001376857.1:c.784_797dup	NM_001376857.1:c.783_797dup	NM_001376857.1:c.797_798insTTTTTTTTTTTTTTTT	NM_001376857.1:c.797_798insTTTTTTTTTTTTTTTTT	NM_001376857.1:c.797_798insTTTTTTTTTTTTTTTTTT	NM_001376857.1:c.797_798insTTTTTTTTTTTTTTTTTTT	NM_001376857.1:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant 3	NM_001376858.1:c.783_797=	NM_001376858.1:c.790_797del	NM_001376858.1:c.791_797del	NM_001376858.1:c.792_797del	NM_001376858.1:c.794_797del	NM_001376858.1:c.795_797del	NM_001376858.1:c.796_797del	NM_001376858.1:c.*797del	NM_001376858.1:c.*797dup	NM_001376858.1:c.796_797dup	NM_001376858.1:c.795_797dup	NM_001376858.1:c.794_797dup	NM_001376858.1:c.793_797dup	NM_001376858.1:c.792_797dup	NM_001376858.1:c.791_797dup	NM_001376858.1:c.790_797dup	NM_001376858.1:c.789_797dup	NM_001376858.1:c.788_797dup	NM_001376858.1:c.785_797dup	NM_001376858.1:c.784_797dup	NM_001376858.1:c.783_797dup	NM_001376858.1:c.797_798insTTTTTTTTTTTTTTTT	NM_001376858.1:c.797_798insTTTTTTTTTTTTTTTTT	NM_001376858.1:c.797_798insTTTTTTTTTTTTTTTTTT	NM_001376858.1:c.797_798insTTTTTTTTTTTTTTTTTTT	NM_001376858.1:c.797_798insTTTTTTTTTTTTTTTTTTTT
TXLNA transcript variant 4	NM_001376859.1:c.783_797=	NM_001376859.1:c.790_797del	NM_001376859.1:c.791_797del	NM_001376859.1:c.792_797del	NM_001376859.1:c.794_797del	NM_001376859.1:c.795_797del	NM_001376859.1:c.796_797del	NM_001376859.1:c.*797del	NM_001376859.1:c.*797dup	NM_001376859.1:c.796_797dup	NM_001376859.1:c.795_797dup	NM_001376859.1:c.794_797dup	NM_001376859.1:c.793_797dup	NM_001376859.1:c.792_797dup	NM_001376859.1:c.791_797dup	NM_001376859.1:c.790_797dup	NM_001376859.1:c.789_797dup	NM_001376859.1:c.788_797dup	NM_001376859.1:c.785_797dup	NM_001376859.1:c.784_797dup	NM_001376859.1:c.783_797dup	NM_001376859.1:c.797_798insTTTTTTTTTTTTTTTT	NM_001376859.1:c.797_798insTTTTTTTTTTTTTTTTT	NM_001376859.1:c.797_798insTTTTTTTTTTTTTTTTTT	NM_001376859.1:c.797_798insTTTTTTTTTTTTTTTTTTT	NM_001376859.1:c.797_798insTTTTTTTTTTTTTTTTTTTT

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs112648110