Name: rs759317254
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.

rs759317254

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:64154957-64154980 (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)₁₄ / del(T)₁₃ / del(T)₁₂ / d…
del(T)₁₄ / del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / 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
Variation Type: Indel Insertion and Deletion
Frequency: dupTT=0.01313 (204/15532, ALFA)
dupT=0.45 (18/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SNX22 : Non Coding Transcript 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	15532	TTTTTTTTTTTTTTTTTTTTTTTT=0.96678	TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00064, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00863, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00747, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.01313, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00142, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00193	0.974092	0.000534	0.025374	4
European	Sub	12896	TTTTTTTTTTTTTTTTTTTTTTTT=0.96007	TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00078, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.01039, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00900, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.01574, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00171, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00233	0.96872	0.000648	0.030632	3
African	Sub	1584	TTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	64	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1520	TTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	112	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
East Asian	Sub	86	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	26	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	98	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	392	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	86	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	364	TTTTTTTTTTTTTTTTTTTTTTTT=0.997	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.003, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.994505	0.0	0.005495	0

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	15532	(T)₂₄=0.96678	del(T)₁₄=0.00000, del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00064, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00863, dupT=0.00747, dupTT=0.01313, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00142, dup(T)₆=0.00193
Allele Frequency Aggregator	European	Sub	12896	(T)₂₄=0.96007	del(T)₁₄=0.00000, del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00078, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.01039, dupT=0.00900, dupTT=0.01574, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00171, dup(T)₆=0.00233
Allele Frequency Aggregator	African	Sub	1584	(T)₂₄=1.0000	del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=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)₅=0.0000, dup(T)₆=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	392	(T)₂₄=1.000	del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=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)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Other	Sub	364	(T)₂₄=0.997	del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.003, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Asian	Sub	112	(T)₂₄=1.000	del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=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)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	98	(T)₂₄=1.00	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=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)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	86	(T)₂₄=1.00	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=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)₅=0.00, dup(T)₆=0.00
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.45

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 15	NC_000015.10:g.64154967_64154980del
GRCh38.p14 chr 15	NC_000015.10:g.64154968_64154980del
GRCh38.p14 chr 15	NC_000015.10:g.64154969_64154980del
GRCh38.p14 chr 15	NC_000015.10:g.64154970_64154980del
GRCh38.p14 chr 15	NC_000015.10:g.64154971_64154980del
GRCh38.p14 chr 15	NC_000015.10:g.64154972_64154980del
GRCh38.p14 chr 15	NC_000015.10:g.64154973_64154980del
GRCh38.p14 chr 15	NC_000015.10:g.64154974_64154980del
GRCh38.p14 chr 15	NC_000015.10:g.64154975_64154980del
GRCh38.p14 chr 15	NC_000015.10:g.64154976_64154980del
GRCh38.p14 chr 15	NC_000015.10:g.64154977_64154980del
GRCh38.p14 chr 15	NC_000015.10:g.64154978_64154980del
GRCh38.p14 chr 15	NC_000015.10:g.64154979_64154980del
GRCh38.p14 chr 15	NC_000015.10:g.64154980del
GRCh38.p14 chr 15	NC_000015.10:g.64154980dup
GRCh38.p14 chr 15	NC_000015.10:g.64154979_64154980dup
GRCh38.p14 chr 15	NC_000015.10:g.64154978_64154980dup
GRCh38.p14 chr 15	NC_000015.10:g.64154977_64154980dup
GRCh38.p14 chr 15	NC_000015.10:g.64154976_64154980dup
GRCh38.p14 chr 15	NC_000015.10:g.64154975_64154980dup
GRCh38.p14 chr 15	NC_000015.10:g.64154974_64154980dup
GRCh38.p14 chr 15	NC_000015.10:g.64154973_64154980dup
GRCh38.p14 chr 15	NC_000015.10:g.64154972_64154980dup
GRCh37.p13 chr 15	NC_000015.9:g.64447166_64447179del
GRCh37.p13 chr 15	NC_000015.9:g.64447167_64447179del
GRCh37.p13 chr 15	NC_000015.9:g.64447168_64447179del
GRCh37.p13 chr 15	NC_000015.9:g.64447169_64447179del
GRCh37.p13 chr 15	NC_000015.9:g.64447170_64447179del
GRCh37.p13 chr 15	NC_000015.9:g.64447171_64447179del
GRCh37.p13 chr 15	NC_000015.9:g.64447172_64447179del
GRCh37.p13 chr 15	NC_000015.9:g.64447173_64447179del
GRCh37.p13 chr 15	NC_000015.9:g.64447174_64447179del
GRCh37.p13 chr 15	NC_000015.9:g.64447175_64447179del
GRCh37.p13 chr 15	NC_000015.9:g.64447176_64447179del
GRCh37.p13 chr 15	NC_000015.9:g.64447177_64447179del
GRCh37.p13 chr 15	NC_000015.9:g.64447178_64447179del
GRCh37.p13 chr 15	NC_000015.9:g.64447179del
GRCh37.p13 chr 15	NC_000015.9:g.64447179dup
GRCh37.p13 chr 15	NC_000015.9:g.64447178_64447179dup
GRCh37.p13 chr 15	NC_000015.9:g.64447177_64447179dup
GRCh37.p13 chr 15	NC_000015.9:g.64447176_64447179dup
GRCh37.p13 chr 15	NC_000015.9:g.64447175_64447179dup
GRCh37.p13 chr 15	NC_000015.9:g.64447174_64447179dup
GRCh37.p13 chr 15	NC_000015.9:g.64447173_64447179dup
GRCh37.p13 chr 15	NC_000015.9:g.64447172_64447179dup
GRCh37.p13 chr 15	NC_000015.9:g.64447171_64447179dup
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13186_13199del
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13187_13199del
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13188_13199del
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13189_13199del
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13190_13199del
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13191_13199del
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13192_13199del
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13193_13199del
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13194_13199del
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13195_13199del
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13196_13199del
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13197_13199del
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13198_13199del
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13199del
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13199dup
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13198_13199dup
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13197_13199dup
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13196_13199dup
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13195_13199dup
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13194_13199dup
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13193_13199dup
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13192_13199dup
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13191_13199dup
SNX22 RefSeqGene	NG_033071.1:g.8251_8264del
SNX22 RefSeqGene	NG_033071.1:g.8252_8264del
SNX22 RefSeqGene	NG_033071.1:g.8253_8264del
SNX22 RefSeqGene	NG_033071.1:g.8254_8264del
SNX22 RefSeqGene	NG_033071.1:g.8255_8264del
SNX22 RefSeqGene	NG_033071.1:g.8256_8264del
SNX22 RefSeqGene	NG_033071.1:g.8257_8264del
SNX22 RefSeqGene	NG_033071.1:g.8258_8264del
SNX22 RefSeqGene	NG_033071.1:g.8259_8264del
SNX22 RefSeqGene	NG_033071.1:g.8260_8264del
SNX22 RefSeqGene	NG_033071.1:g.8261_8264del
SNX22 RefSeqGene	NG_033071.1:g.8262_8264del
SNX22 RefSeqGene	NG_033071.1:g.8263_8264del
SNX22 RefSeqGene	NG_033071.1:g.8264del
SNX22 RefSeqGene	NG_033071.1:g.8264dup
SNX22 RefSeqGene	NG_033071.1:g.8263_8264dup
SNX22 RefSeqGene	NG_033071.1:g.8262_8264dup
SNX22 RefSeqGene	NG_033071.1:g.8261_8264dup
SNX22 RefSeqGene	NG_033071.1:g.8260_8264dup
SNX22 RefSeqGene	NG_033071.1:g.8259_8264dup
SNX22 RefSeqGene	NG_033071.1:g.8258_8264dup
SNX22 RefSeqGene	NG_033071.1:g.8257_8264dup
SNX22 RefSeqGene	NG_033071.1:g.8256_8264dup

Gene: SNX22, sorting nexin 22 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SNX22 transcript variant 1	NM_024798.3:c.449_472=	N/A	3 Prime UTR Variant
SNX22 transcript variant 2	NR_073534.2:n.1133_1146del	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1134_1146del	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1135_1146del	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1136_1146del	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1137_1146del	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1138_1146del	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1139_1146del	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1140_1146del	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1141_1146del	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1142_1146del	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1143_1146del	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1144_1146del	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1145_1146del	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1146del	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1146dup	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1145_1146dup	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1144_1146dup	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1143_1146dup	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1142_1146dup	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1141_1146dup	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1140_1146dup	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1139_1146dup	N/A	Non Coding Transcript Variant
SNX22 transcript variant 2	NR_073534.2:n.1138_1146dup	N/A	Non Coding Transcript Variant
SNX22 transcript variant X2	XM_017022581.2:c.449_47… XM_017022581.2:c.449_472=	N/A	3 Prime UTR Variant
SNX22 transcript variant X1	XM_005254677.4:c.	N/A	Genic Downstream 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)₂₄=	del(T)₁₄	del(T)₁₃	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	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
GRCh38.p14 chr 15	NC_000015.10:g.64154957_64154980=	NC_000015.10:g.64154967_64154980del	NC_000015.10:g.64154968_64154980del	NC_000015.10:g.64154969_64154980del	NC_000015.10:g.64154970_64154980del	NC_000015.10:g.64154971_64154980del	NC_000015.10:g.64154972_64154980del	NC_000015.10:g.64154973_64154980del	NC_000015.10:g.64154974_64154980del	NC_000015.10:g.64154975_64154980del	NC_000015.10:g.64154976_64154980del	NC_000015.10:g.64154977_64154980del	NC_000015.10:g.64154978_64154980del	NC_000015.10:g.64154979_64154980del	NC_000015.10:g.64154980del	NC_000015.10:g.64154980dup	NC_000015.10:g.64154979_64154980dup	NC_000015.10:g.64154978_64154980dup	NC_000015.10:g.64154977_64154980dup	NC_000015.10:g.64154976_64154980dup	NC_000015.10:g.64154975_64154980dup	NC_000015.10:g.64154974_64154980dup	NC_000015.10:g.64154973_64154980dup	NC_000015.10:g.64154972_64154980dup
GRCh37.p13 chr 15	NC_000015.9:g.64447156_64447179=	NC_000015.9:g.64447166_64447179del	NC_000015.9:g.64447167_64447179del	NC_000015.9:g.64447168_64447179del	NC_000015.9:g.64447169_64447179del	NC_000015.9:g.64447170_64447179del	NC_000015.9:g.64447171_64447179del	NC_000015.9:g.64447172_64447179del	NC_000015.9:g.64447173_64447179del	NC_000015.9:g.64447174_64447179del	NC_000015.9:g.64447175_64447179del	NC_000015.9:g.64447176_64447179del	NC_000015.9:g.64447177_64447179del	NC_000015.9:g.64447178_64447179del	NC_000015.9:g.64447179del	NC_000015.9:g.64447179dup	NC_000015.9:g.64447178_64447179dup	NC_000015.9:g.64447177_64447179dup	NC_000015.9:g.64447176_64447179dup	NC_000015.9:g.64447175_64447179dup	NC_000015.9:g.64447174_64447179dup	NC_000015.9:g.64447173_64447179dup	NC_000015.9:g.64447172_64447179dup	NC_000015.9:g.64447171_64447179dup
PPIB RefSeqGene (LRG_10)	NG_012979.1:g.13176_13199=	NG_012979.1:g.13186_13199del	NG_012979.1:g.13187_13199del	NG_012979.1:g.13188_13199del	NG_012979.1:g.13189_13199del	NG_012979.1:g.13190_13199del	NG_012979.1:g.13191_13199del	NG_012979.1:g.13192_13199del	NG_012979.1:g.13193_13199del	NG_012979.1:g.13194_13199del	NG_012979.1:g.13195_13199del	NG_012979.1:g.13196_13199del	NG_012979.1:g.13197_13199del	NG_012979.1:g.13198_13199del	NG_012979.1:g.13199del	NG_012979.1:g.13199dup	NG_012979.1:g.13198_13199dup	NG_012979.1:g.13197_13199dup	NG_012979.1:g.13196_13199dup	NG_012979.1:g.13195_13199dup	NG_012979.1:g.13194_13199dup	NG_012979.1:g.13193_13199dup	NG_012979.1:g.13192_13199dup	NG_012979.1:g.13191_13199dup
SNX22 RefSeqGene	NG_033071.1:g.8241_8264=	NG_033071.1:g.8251_8264del	NG_033071.1:g.8252_8264del	NG_033071.1:g.8253_8264del	NG_033071.1:g.8254_8264del	NG_033071.1:g.8255_8264del	NG_033071.1:g.8256_8264del	NG_033071.1:g.8257_8264del	NG_033071.1:g.8258_8264del	NG_033071.1:g.8259_8264del	NG_033071.1:g.8260_8264del	NG_033071.1:g.8261_8264del	NG_033071.1:g.8262_8264del	NG_033071.1:g.8263_8264del	NG_033071.1:g.8264del	NG_033071.1:g.8264dup	NG_033071.1:g.8263_8264dup	NG_033071.1:g.8262_8264dup	NG_033071.1:g.8261_8264dup	NG_033071.1:g.8260_8264dup	NG_033071.1:g.8259_8264dup	NG_033071.1:g.8258_8264dup	NG_033071.1:g.8257_8264dup	NG_033071.1:g.8256_8264dup
SNX22 transcript variant 1	NM_024798.3:c.449_472=	NM_024798.3:c.459_472del	NM_024798.3:c.460_472del	NM_024798.3:c.461_472del	NM_024798.3:c.462_472del	NM_024798.3:c.463_472del	NM_024798.3:c.464_472del	NM_024798.3:c.465_472del	NM_024798.3:c.466_472del	NM_024798.3:c.467_472del	NM_024798.3:c.468_472del	NM_024798.3:c.469_472del	NM_024798.3:c.470_472del	NM_024798.3:c.471_472del	NM_024798.3:c.*472del	NM_024798.3:c.*472dup	NM_024798.3:c.471_472dup	NM_024798.3:c.470_472dup	NM_024798.3:c.469_472dup	NM_024798.3:c.468_472dup	NM_024798.3:c.467_472dup	NM_024798.3:c.466_472dup	NM_024798.3:c.465_472dup	NM_024798.3:c.464_472dup
SNX22 transcript variant 1	NM_024798.2:c.449_472=	NM_024798.2:c.459_472del	NM_024798.2:c.460_472del	NM_024798.2:c.461_472del	NM_024798.2:c.462_472del	NM_024798.2:c.463_472del	NM_024798.2:c.464_472del	NM_024798.2:c.465_472del	NM_024798.2:c.466_472del	NM_024798.2:c.467_472del	NM_024798.2:c.468_472del	NM_024798.2:c.469_472del	NM_024798.2:c.470_472del	NM_024798.2:c.471_472del	NM_024798.2:c.*472del	NM_024798.2:c.*472dup	NM_024798.2:c.471_472dup	NM_024798.2:c.470_472dup	NM_024798.2:c.469_472dup	NM_024798.2:c.468_472dup	NM_024798.2:c.467_472dup	NM_024798.2:c.466_472dup	NM_024798.2:c.465_472dup	NM_024798.2:c.464_472dup
SNX22 transcript variant 2	NR_073534.2:n.1123_1146=	NR_073534.2:n.1133_1146del	NR_073534.2:n.1134_1146del	NR_073534.2:n.1135_1146del	NR_073534.2:n.1136_1146del	NR_073534.2:n.1137_1146del	NR_073534.2:n.1138_1146del	NR_073534.2:n.1139_1146del	NR_073534.2:n.1140_1146del	NR_073534.2:n.1141_1146del	NR_073534.2:n.1142_1146del	NR_073534.2:n.1143_1146del	NR_073534.2:n.1144_1146del	NR_073534.2:n.1145_1146del	NR_073534.2:n.1146del	NR_073534.2:n.1146dup	NR_073534.2:n.1145_1146dup	NR_073534.2:n.1144_1146dup	NR_073534.2:n.1143_1146dup	NR_073534.2:n.1142_1146dup	NR_073534.2:n.1141_1146dup	NR_073534.2:n.1140_1146dup	NR_073534.2:n.1139_1146dup	NR_073534.2:n.1138_1146dup
SNX22 transcript variant 2	NR_073534.1:n.1137_1160=	NR_073534.1:n.1147_1160del	NR_073534.1:n.1148_1160del	NR_073534.1:n.1149_1160del	NR_073534.1:n.1150_1160del	NR_073534.1:n.1151_1160del	NR_073534.1:n.1152_1160del	NR_073534.1:n.1153_1160del	NR_073534.1:n.1154_1160del	NR_073534.1:n.1155_1160del	NR_073534.1:n.1156_1160del	NR_073534.1:n.1157_1160del	NR_073534.1:n.1158_1160del	NR_073534.1:n.1159_1160del	NR_073534.1:n.1160del	NR_073534.1:n.1160dup	NR_073534.1:n.1159_1160dup	NR_073534.1:n.1158_1160dup	NR_073534.1:n.1157_1160dup	NR_073534.1:n.1156_1160dup	NR_073534.1:n.1155_1160dup	NR_073534.1:n.1154_1160dup	NR_073534.1:n.1153_1160dup	NR_073534.1:n.1152_1160dup
SNX22 transcript variant X2	XM_017022581.2:c.449_472=	XM_017022581.2:c.459_472del	XM_017022581.2:c.460_472del	XM_017022581.2:c.461_472del	XM_017022581.2:c.462_472del	XM_017022581.2:c.463_472del	XM_017022581.2:c.464_472del	XM_017022581.2:c.465_472del	XM_017022581.2:c.466_472del	XM_017022581.2:c.467_472del	XM_017022581.2:c.468_472del	XM_017022581.2:c.469_472del	XM_017022581.2:c.470_472del	XM_017022581.2:c.471_472del	XM_017022581.2:c.*472del	XM_017022581.2:c.*472dup	XM_017022581.2:c.471_472dup	XM_017022581.2:c.470_472dup	XM_017022581.2:c.469_472dup	XM_017022581.2:c.468_472dup	XM_017022581.2:c.467_472dup	XM_017022581.2:c.466_472dup	XM_017022581.2:c.465_472dup	XM_017022581.2:c.464_472dup
SNX22 transcript variant X2	XM_017022581.1:c.449_472=	XM_017022581.1:c.459_472del	XM_017022581.1:c.460_472del	XM_017022581.1:c.461_472del	XM_017022581.1:c.462_472del	XM_017022581.1:c.463_472del	XM_017022581.1:c.464_472del	XM_017022581.1:c.465_472del	XM_017022581.1:c.466_472del	XM_017022581.1:c.467_472del	XM_017022581.1:c.468_472del	XM_017022581.1:c.469_472del	XM_017022581.1:c.470_472del	XM_017022581.1:c.471_472del	XM_017022581.1:c.*472del	XM_017022581.1:c.*472dup	XM_017022581.1:c.471_472dup	XM_017022581.1:c.470_472dup	XM_017022581.1:c.469_472dup	XM_017022581.1:c.468_472dup	XM_017022581.1:c.467_472dup	XM_017022581.1:c.466_472dup	XM_017022581.1:c.465_472dup	XM_017022581.1:c.464_472dup

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#.

49 SubSNP, 36 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCMHGSC_JDW	ss103577453	Mar 15, 2016 (147)
2	SSMP	ss664281315	Apr 01, 2015 (144)
3	EVA_GENOME_DK	ss1574872798	Apr 01, 2015 (144)
4	SWEGEN	ss3013432548	Nov 08, 2017 (151)
5	PACBIO	ss3792882398	Jul 13, 2019 (153)
6	PACBIO	ss3797766977	Jul 13, 2019 (153)
7	KOGIC	ss3976326173	Apr 27, 2020 (154)
8	KOGIC	ss3976326174	Apr 27, 2020 (154)
9	KOGIC	ss3976326175	Apr 27, 2020 (154)
10	KOGIC	ss3976326176	Apr 27, 2020 (154)
11	GNOMAD	ss4290396635	Apr 27, 2021 (155)
12	GNOMAD	ss4290396636	Apr 27, 2021 (155)
13	GNOMAD	ss4290396637	Apr 27, 2021 (155)
14	GNOMAD	ss4290396638	Apr 27, 2021 (155)
15	GNOMAD	ss4290396639	Apr 27, 2021 (155)
16	GNOMAD	ss4290396640	Apr 27, 2021 (155)
17	GNOMAD	ss4290396641	Apr 27, 2021 (155)
18	GNOMAD	ss4290396643	Apr 27, 2021 (155)
19	GNOMAD	ss4290396644	Apr 27, 2021 (155)
20	GNOMAD	ss4290396645	Apr 27, 2021 (155)
21	GNOMAD	ss4290396646	Apr 27, 2021 (155)
22	GNOMAD	ss4290396647	Apr 27, 2021 (155)
23	GNOMAD	ss4290396648	Apr 27, 2021 (155)
24	GNOMAD	ss4290396649	Apr 27, 2021 (155)
25	GNOMAD	ss4290396650	Apr 27, 2021 (155)
26	GNOMAD	ss4290396651	Apr 27, 2021 (155)
27	GNOMAD	ss4290396652	Apr 27, 2021 (155)
28	GNOMAD	ss4290396653	Apr 27, 2021 (155)
29	GNOMAD	ss4290396654	Apr 27, 2021 (155)
30	GNOMAD	ss4290396655	Apr 27, 2021 (155)
31	GNOMAD	ss4290396656	Apr 27, 2021 (155)
32	TOMMO_GENOMICS	ss5216621211	Apr 27, 2021 (155)
33	TOMMO_GENOMICS	ss5216621212	Apr 27, 2021 (155)
34	TOMMO_GENOMICS	ss5216621213	Apr 27, 2021 (155)
35	TOMMO_GENOMICS	ss5216621214	Apr 27, 2021 (155)
36	1000G_HIGH_COVERAGE	ss5298767350	Oct 16, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5298767351	Oct 16, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5298767352	Oct 16, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5298767353	Oct 16, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5298767354	Oct 16, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5298767355	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5492464844	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5492464845	Oct 16, 2022 (156)
44	SANFORD_IMAGENETICS	ss5657696471	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5770550578	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5770550579	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5770550580	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5770550581	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5770550582	Oct 16, 2022 (156)
50	The Danish reference pan genome	NC_000015.9 - 64447156	Apr 27, 2020 (154)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471789839 (NC_000015.10:64154956::TTT 229/75792) Row 471789840 (NC_000015.10:64154956::TTTT 64/75810) Row 471789841 (NC_000015.10:64154956::TTTTT 33/75806)...	-	Apr 27, 2021 (155)
72	Korean Genome Project Submission ignored due to conflicting rows: Row 32704174 (NC_000015.10:64154956:TT: 15/1812) Row 32704175 (NC_000015.10:64154958::TT 63/1812) Row 32704176 (NC_000015.10:64154958::T 260/1812)...	-	Apr 27, 2020 (154)
73	Korean Genome Project Submission ignored due to conflicting rows: Row 32704174 (NC_000015.10:64154956:TT: 15/1812) Row 32704175 (NC_000015.10:64154958::TT 63/1812) Row 32704176 (NC_000015.10:64154958::T 260/1812)...	-	Apr 27, 2020 (154)
74	Korean Genome Project Submission ignored due to conflicting rows: Row 32704174 (NC_000015.10:64154956:TT: 15/1812) Row 32704175 (NC_000015.10:64154958::TT 63/1812) Row 32704176 (NC_000015.10:64154958::T 260/1812)...	-	Apr 27, 2020 (154)
75	Korean Genome Project Submission ignored due to conflicting rows: Row 32704174 (NC_000015.10:64154956:TT: 15/1812) Row 32704175 (NC_000015.10:64154958::TT 63/1812) Row 32704176 (NC_000015.10:64154958::T 260/1812)...	-	Apr 27, 2020 (154)
76	8.3KJPN Submission ignored due to conflicting rows: Row 74590518 (NC_000015.9:64447155::T 188/16504) Row 74590519 (NC_000015.9:64447155::TT 212/16504) Row 74590520 (NC_000015.9:64447155:TTTTTTT: 2/16504)...	-	Apr 27, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 74590518 (NC_000015.9:64447155::T 188/16504) Row 74590519 (NC_000015.9:64447155::TT 212/16504) Row 74590520 (NC_000015.9:64447155:TTTTTTT: 2/16504)...	-	Apr 27, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 74590518 (NC_000015.9:64447155::T 188/16504) Row 74590519 (NC_000015.9:64447155::TT 212/16504) Row 74590520 (NC_000015.9:64447155:TTTTTTT: 2/16504)...	-	Apr 27, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 74590518 (NC_000015.9:64447155::T 188/16504) Row 74590519 (NC_000015.9:64447155::TT 212/16504) Row 74590520 (NC_000015.9:64447155:TTTTTTT: 2/16504)...	-	Apr 27, 2021 (155)
80	14KJPN Submission ignored due to conflicting rows: Row 104387682 (NC_000015.10:64154956::T 184/27914) Row 104387683 (NC_000015.10:64154956:TTTTTTT: 2/27914) Row 104387684 (NC_000015.10:64154956::TT 182/27914)...	-	Oct 16, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 104387682 (NC_000015.10:64154956::T 184/27914) Row 104387683 (NC_000015.10:64154956:TTTTTTT: 2/27914) Row 104387684 (NC_000015.10:64154956::TT 182/27914)...	-	Oct 16, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 104387682 (NC_000015.10:64154956::T 184/27914) Row 104387683 (NC_000015.10:64154956:TTTTTTT: 2/27914) Row 104387684 (NC_000015.10:64154956::TT 182/27914)...	-	Oct 16, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 104387682 (NC_000015.10:64154956::T 184/27914) Row 104387683 (NC_000015.10:64154956:TTTTTTT: 2/27914) Row 104387684 (NC_000015.10:64154956::TT 182/27914)...	-	Oct 16, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 104387682 (NC_000015.10:64154956::T 184/27914) Row 104387683 (NC_000015.10:64154956:TTTTTTT: 2/27914) Row 104387684 (NC_000015.10:64154956::TT 182/27914)...	-	Oct 16, 2022 (156)
85	ALFA	NC_000015.10 - 64154957	Apr 27, 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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4290396656, ss5298767353	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTT:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4290396655	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTT:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4290396654	NC_000015.10:64154956:TTTTTTTTTTTT:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4290396653	NC_000015.10:64154956:TTTTTTTTTTT:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4290396652	NC_000015.10:64154956:TTTTTTTTTT:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4290396651, ss5770550582	NC_000015.10:64154956:TTTTTTTTT:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4290396650	NC_000015.10:64154956:TTTTTTTT:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3013432548, ss5216621213	NC_000015.9:64447155:TTTTTTT:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4290396649, ss5298767354, ss5770550579	NC_000015.10:64154956:TTTTTTT:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4290396648, ss5298767355	NC_000015.10:64154956:TTTTTT:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4290396647	NC_000015.10:64154956:TTTTT:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4290396646	NC_000015.10:64154956:TTTT:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4290396645	NC_000015.10:64154956:TTT:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3976326173, ss4290396644	NC_000015.10:64154956:TT:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5216621214, ss5657696471	NC_000015.9:64447155:T:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4290396643, ss5298767352, ss5492464845, ss5770550581	NC_000015.10:64154956:T:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3976326176	NC_000015.10:64154957:T:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
494717, ss664281315, ss1574872798, ss3792882398, ss3797766977, ss5216621211	NC_000015.9:64447155::T	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5298767351, ss5492464844, ss5770550578	NC_000015.10:64154956::T	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3976326175	NC_000015.10:64154958::T	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5216621212	NC_000015.9:64447155::TT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5298767350, ss5770550580	NC_000015.10:64154956::TT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3976326174	NC_000015.10:64154958::TT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss103577453	NT_010194.17:35237736:G:TTG	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4290396635	NC_000015.10:64154956::TTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4290396636	NC_000015.10:64154956::TTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4290396637	NC_000015.10:64154956::TTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4290396638	NC_000015.10:64154956::TTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10059672878	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4290396639	NC_000015.10:64154956::TTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4290396640	NC_000015.10:64154956::TTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4290396641	NC_000015.10:64154956::TTTTTTTTT	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2371993304	NC_000015.9:64447155:TTTTTTTTTTTT:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT
ss2371993305	NC_000015.9:64447155:TTTTTTTTTTTTT… NC_000015.9:64447155:TTTTTTTTTTTTTT:	NC_000015.10:64154956:TTTTTTTTTTTT… NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT

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

No publications for rs759317254

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

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs759317254