Name: rs764051983
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.

rs764051983

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:60232477-60232496 (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)₁₀ / del(T)₇ / del(T)₆ / del…
del(T)₁₀ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / ins(T)₂₅ / ins(T)₂₆
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.00948 (147/15514, ALFA)
delT=0.38 (15/40, GENOME_DK)
dupT=0.2 (2/8, KOREAN)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: USP32 : Intron Variant
SCARNA20 : 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	15514	TTTTTTTTTTTTTTTTTTTT=0.98846	TTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00200, TTTTTTTTTTTTTTTTTTTTT=0.00948, TTTTTTTTTTTTTTTTTTTTTT=0.00006, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.981877	0.000777	0.017346	22
European	Sub	13172	TTTTTTTTTTTTTTTTTTTT=0.98641	TTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00235, TTTTTTTTTTTTTTTTTTTTT=0.01116, TTTTTTTTTTTTTTTTTTTTTT=0.00008, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.978639	0.000915	0.020446	18
African	Sub	1208	TTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	40	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1168	TTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	100	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	82	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	18	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	100	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	482	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	80	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	372	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=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	15514	(T)₂₀=0.98846	del(T)₁₀=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, delTT=0.00000, delT=0.00200, dupT=0.00948, dupTT=0.00006, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00000, dup(T)₆=0.00000, dup(T)₇=0.00000
Allele Frequency Aggregator	European	Sub	13172	(T)₂₀=0.98641	del(T)₁₀=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, delTT=0.00000, delT=0.00235, dupT=0.01116, dupTT=0.00008, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00000, dup(T)₆=0.00000, dup(T)₇=0.00000
Allele Frequency Aggregator	African	Sub	1208	(T)₂₀=1.0000	del(T)₁₀=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=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, dup(T)₇=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	482	(T)₂₀=1.000	del(T)₁₀=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=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, dup(T)₇=0.000
Allele Frequency Aggregator	Other	Sub	372	(T)₂₀=1.000	del(T)₁₀=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=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, dup(T)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	100	(T)₂₀=1.00	del(T)₁₀=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=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, dup(T)₇=0.00
Allele Frequency Aggregator	Asian	Sub	100	(T)₂₀=1.00	del(T)₁₀=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=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, dup(T)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	80	(T)₂₀=1.00	del(T)₁₀=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=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, dup(T)₇=0.00
The Danish reference pan genome	Danish	Study-wide	40	(T)₂₀=0.62	delT=0.38
KOREAN population from KRGDB	KOREAN	Study-wide	8	- No frequency provided	dupT=0.2

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 17	NC_000017.11:g.60232487_60232496del
GRCh38.p14 chr 17	NC_000017.11:g.60232490_60232496del
GRCh38.p14 chr 17	NC_000017.11:g.60232491_60232496del
GRCh38.p14 chr 17	NC_000017.11:g.60232492_60232496del
GRCh38.p14 chr 17	NC_000017.11:g.60232493_60232496del
GRCh38.p14 chr 17	NC_000017.11:g.60232495_60232496del
GRCh38.p14 chr 17	NC_000017.11:g.60232496del
GRCh38.p14 chr 17	NC_000017.11:g.60232496dup
GRCh38.p14 chr 17	NC_000017.11:g.60232495_60232496dup
GRCh38.p14 chr 17	NC_000017.11:g.60232494_60232496dup
GRCh38.p14 chr 17	NC_000017.11:g.60232493_60232496dup
GRCh38.p14 chr 17	NC_000017.11:g.60232492_60232496dup
GRCh38.p14 chr 17	NC_000017.11:g.60232491_60232496dup
GRCh38.p14 chr 17	NC_000017.11:g.60232490_60232496dup
GRCh38.p14 chr 17	NC_000017.11:g.60232496_60232497insTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 17	NC_000017.11:g.60232496_60232497insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.58309848_58309857del
GRCh37.p13 chr 17	NC_000017.10:g.58309851_58309857del
GRCh37.p13 chr 17	NC_000017.10:g.58309852_58309857del
GRCh37.p13 chr 17	NC_000017.10:g.58309853_58309857del
GRCh37.p13 chr 17	NC_000017.10:g.58309854_58309857del
GRCh37.p13 chr 17	NC_000017.10:g.58309856_58309857del
GRCh37.p13 chr 17	NC_000017.10:g.58309857del
GRCh37.p13 chr 17	NC_000017.10:g.58309857dup
GRCh37.p13 chr 17	NC_000017.10:g.58309856_58309857dup
GRCh37.p13 chr 17	NC_000017.10:g.58309855_58309857dup
GRCh37.p13 chr 17	NC_000017.10:g.58309854_58309857dup
GRCh37.p13 chr 17	NC_000017.10:g.58309853_58309857dup
GRCh37.p13 chr 17	NC_000017.10:g.58309852_58309857dup
GRCh37.p13 chr 17	NC_000017.10:g.58309851_58309857dup
GRCh37.p13 chr 17	NC_000017.10:g.58309857_58309858insTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.58309857_58309858insTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: USP32, ubiquitin specific peptidase 32 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
USP32 transcript	NM_032582.4:c.1239+3652_1… NM_032582.4:c.1239+3652_1239+3661del	N/A	Intron Variant
USP32 transcript variant X1	XM_011525371.2:c.1287+365… XM_011525371.2:c.1287+3652_1287+3661del	N/A	Intron Variant
USP32 transcript variant X2	XM_011525372.2:c.1287+365… XM_011525372.2:c.1287+3652_1287+3661del	N/A	Intron Variant
USP32 transcript variant X3	XM_011525373.2:c.1239+365… XM_011525373.2:c.1239+3652_1239+3661del	N/A	Intron Variant
USP32 transcript variant X4	XM_011525374.2:c.1230+365… XM_011525374.2:c.1230+3652_1230+3661del	N/A	Intron Variant
USP32 transcript variant X5	XM_011525375.2:c.1209+365… XM_011525375.2:c.1209+3652_1209+3661del	N/A	Intron Variant
USP32 transcript variant X6	XM_011525376.2:c.1230+365… XM_011525376.2:c.1230+3652_1230+3661del	N/A	Intron Variant
USP32 transcript variant X8	XM_011525378.2:c.1101+365… XM_011525378.2:c.1101+3652_1101+3661del	N/A	Intron Variant
USP32 transcript variant X11	XM_011525379.4:c.366+3652… XM_011525379.4:c.366+3652_366+3661del	N/A	Intron Variant
USP32 transcript variant X9	XM_017025233.2:c.1101+365… XM_017025233.2:c.1101+3652_1101+3661del	N/A	Intron Variant
USP32 transcript variant X7	XM_047436943.1:c.1209+365… XM_047436943.1:c.1209+3652_1209+3661del	N/A	Intron Variant
USP32 transcript variant X10	XM_047436944.1:c.894+3652… XM_047436944.1:c.894+3652_894+3661del	N/A	Intron Variant
USP32 transcript variant X12	XM_047436945.1:c.324+3652… XM_047436945.1:c.324+3652_324+3661del	N/A	Intron Variant

Gene: SCARNA20, small Cajal body-specific RNA 20 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
SCARNA20 transcript	NR_002999.2:n.	N/A	Upstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(T)₂₀=	del(T)₁₀	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	ins(T)₂₅	ins(T)₂₆
GRCh38.p14 chr 17	NC_000017.11:g.60232477_60232496=	NC_000017.11:g.60232487_60232496del	NC_000017.11:g.60232490_60232496del	NC_000017.11:g.60232491_60232496del	NC_000017.11:g.60232492_60232496del	NC_000017.11:g.60232493_60232496del	NC_000017.11:g.60232495_60232496del	NC_000017.11:g.60232496del	NC_000017.11:g.60232496dup	NC_000017.11:g.60232495_60232496dup	NC_000017.11:g.60232494_60232496dup	NC_000017.11:g.60232493_60232496dup	NC_000017.11:g.60232492_60232496dup	NC_000017.11:g.60232491_60232496dup	NC_000017.11:g.60232490_60232496dup	NC_000017.11:g.60232496_60232497insTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:g.60232496_60232497insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.58309838_58309857=	NC_000017.10:g.58309848_58309857del	NC_000017.10:g.58309851_58309857del	NC_000017.10:g.58309852_58309857del	NC_000017.10:g.58309853_58309857del	NC_000017.10:g.58309854_58309857del	NC_000017.10:g.58309856_58309857del	NC_000017.10:g.58309857del	NC_000017.10:g.58309857dup	NC_000017.10:g.58309856_58309857dup	NC_000017.10:g.58309855_58309857dup	NC_000017.10:g.58309854_58309857dup	NC_000017.10:g.58309853_58309857dup	NC_000017.10:g.58309852_58309857dup	NC_000017.10:g.58309851_58309857dup	NC_000017.10:g.58309857_58309858insTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.10:g.58309857_58309858insTTTTTTTTTTTTTTTTTTTTTTTTTT
USP32 transcript	NM_032582.3:c.1239+3661=	NM_032582.3:c.1239+3652_1239+3661del	NM_032582.3:c.1239+3655_1239+3661del	NM_032582.3:c.1239+3656_1239+3661del	NM_032582.3:c.1239+3657_1239+3661del	NM_032582.3:c.1239+3658_1239+3661del	NM_032582.3:c.1239+3660_1239+3661del	NM_032582.3:c.1239+3661del	NM_032582.3:c.1239+3661dup	NM_032582.3:c.1239+3660_1239+3661dup	NM_032582.3:c.1239+3659_1239+3661dup	NM_032582.3:c.1239+3658_1239+3661dup	NM_032582.3:c.1239+3657_1239+3661dup	NM_032582.3:c.1239+3656_1239+3661dup	NM_032582.3:c.1239+3655_1239+3661dup	NM_032582.3:c.1239+3661_1239+3662insAAAAAAAAAAAAAAAAAAAAAAAAA	NM_032582.3:c.1239+3661_1239+3662insAAAAAAAAAAAAAAAAAAAAAAAAAA
USP32 transcript	NM_032582.4:c.1239+3661=	NM_032582.4:c.1239+3652_1239+3661del	NM_032582.4:c.1239+3655_1239+3661del	NM_032582.4:c.1239+3656_1239+3661del	NM_032582.4:c.1239+3657_1239+3661del	NM_032582.4:c.1239+3658_1239+3661del	NM_032582.4:c.1239+3660_1239+3661del	NM_032582.4:c.1239+3661del	NM_032582.4:c.1239+3661dup	NM_032582.4:c.1239+3660_1239+3661dup	NM_032582.4:c.1239+3659_1239+3661dup	NM_032582.4:c.1239+3658_1239+3661dup	NM_032582.4:c.1239+3657_1239+3661dup	NM_032582.4:c.1239+3656_1239+3661dup	NM_032582.4:c.1239+3655_1239+3661dup	NM_032582.4:c.1239+3661_1239+3662insAAAAAAAAAAAAAAAAAAAAAAAAA	NM_032582.4:c.1239+3661_1239+3662insAAAAAAAAAAAAAAAAAAAAAAAAAA
USP32 transcript variant X1	XM_005257738.1:c.249+3661=	XM_005257738.1:c.249+3652_249+3661del	XM_005257738.1:c.249+3655_249+3661del	XM_005257738.1:c.249+3656_249+3661del	XM_005257738.1:c.249+3657_249+3661del	XM_005257738.1:c.249+3658_249+3661del	XM_005257738.1:c.249+3660_249+3661del	XM_005257738.1:c.249+3661del	XM_005257738.1:c.249+3661dup	XM_005257738.1:c.249+3660_249+3661dup	XM_005257738.1:c.249+3659_249+3661dup	XM_005257738.1:c.249+3658_249+3661dup	XM_005257738.1:c.249+3657_249+3661dup	XM_005257738.1:c.249+3656_249+3661dup	XM_005257738.1:c.249+3655_249+3661dup	XM_005257738.1:c.249+3661_249+3662insAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005257738.1:c.249+3661_249+3662insAAAAAAAAAAAAAAAAAAAAAAAAAA
USP32 transcript variant X1	XM_011525371.2:c.1287+3661=	XM_011525371.2:c.1287+3652_1287+3661del	XM_011525371.2:c.1287+3655_1287+3661del	XM_011525371.2:c.1287+3656_1287+3661del	XM_011525371.2:c.1287+3657_1287+3661del	XM_011525371.2:c.1287+3658_1287+3661del	XM_011525371.2:c.1287+3660_1287+3661del	XM_011525371.2:c.1287+3661del	XM_011525371.2:c.1287+3661dup	XM_011525371.2:c.1287+3660_1287+3661dup	XM_011525371.2:c.1287+3659_1287+3661dup	XM_011525371.2:c.1287+3658_1287+3661dup	XM_011525371.2:c.1287+3657_1287+3661dup	XM_011525371.2:c.1287+3656_1287+3661dup	XM_011525371.2:c.1287+3655_1287+3661dup	XM_011525371.2:c.1287+3661_1287+3662insAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011525371.2:c.1287+3661_1287+3662insAAAAAAAAAAAAAAAAAAAAAAAAAA
USP32 transcript variant X2	XM_011525372.2:c.1287+3661=	XM_011525372.2:c.1287+3652_1287+3661del	XM_011525372.2:c.1287+3655_1287+3661del	XM_011525372.2:c.1287+3656_1287+3661del	XM_011525372.2:c.1287+3657_1287+3661del	XM_011525372.2:c.1287+3658_1287+3661del	XM_011525372.2:c.1287+3660_1287+3661del	XM_011525372.2:c.1287+3661del	XM_011525372.2:c.1287+3661dup	XM_011525372.2:c.1287+3660_1287+3661dup	XM_011525372.2:c.1287+3659_1287+3661dup	XM_011525372.2:c.1287+3658_1287+3661dup	XM_011525372.2:c.1287+3657_1287+3661dup	XM_011525372.2:c.1287+3656_1287+3661dup	XM_011525372.2:c.1287+3655_1287+3661dup	XM_011525372.2:c.1287+3661_1287+3662insAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011525372.2:c.1287+3661_1287+3662insAAAAAAAAAAAAAAAAAAAAAAAAAA
USP32 transcript variant X3	XM_011525373.2:c.1239+3661=	XM_011525373.2:c.1239+3652_1239+3661del	XM_011525373.2:c.1239+3655_1239+3661del	XM_011525373.2:c.1239+3656_1239+3661del	XM_011525373.2:c.1239+3657_1239+3661del	XM_011525373.2:c.1239+3658_1239+3661del	XM_011525373.2:c.1239+3660_1239+3661del	XM_011525373.2:c.1239+3661del	XM_011525373.2:c.1239+3661dup	XM_011525373.2:c.1239+3660_1239+3661dup	XM_011525373.2:c.1239+3659_1239+3661dup	XM_011525373.2:c.1239+3658_1239+3661dup	XM_011525373.2:c.1239+3657_1239+3661dup	XM_011525373.2:c.1239+3656_1239+3661dup	XM_011525373.2:c.1239+3655_1239+3661dup	XM_011525373.2:c.1239+3661_1239+3662insAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011525373.2:c.1239+3661_1239+3662insAAAAAAAAAAAAAAAAAAAAAAAAAA
USP32 transcript variant X4	XM_011525374.2:c.1230+3661=	XM_011525374.2:c.1230+3652_1230+3661del	XM_011525374.2:c.1230+3655_1230+3661del	XM_011525374.2:c.1230+3656_1230+3661del	XM_011525374.2:c.1230+3657_1230+3661del	XM_011525374.2:c.1230+3658_1230+3661del	XM_011525374.2:c.1230+3660_1230+3661del	XM_011525374.2:c.1230+3661del	XM_011525374.2:c.1230+3661dup	XM_011525374.2:c.1230+3660_1230+3661dup	XM_011525374.2:c.1230+3659_1230+3661dup	XM_011525374.2:c.1230+3658_1230+3661dup	XM_011525374.2:c.1230+3657_1230+3661dup	XM_011525374.2:c.1230+3656_1230+3661dup	XM_011525374.2:c.1230+3655_1230+3661dup	XM_011525374.2:c.1230+3661_1230+3662insAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011525374.2:c.1230+3661_1230+3662insAAAAAAAAAAAAAAAAAAAAAAAAAA
USP32 transcript variant X5	XM_011525375.2:c.1209+3661=	XM_011525375.2:c.1209+3652_1209+3661del	XM_011525375.2:c.1209+3655_1209+3661del	XM_011525375.2:c.1209+3656_1209+3661del	XM_011525375.2:c.1209+3657_1209+3661del	XM_011525375.2:c.1209+3658_1209+3661del	XM_011525375.2:c.1209+3660_1209+3661del	XM_011525375.2:c.1209+3661del	XM_011525375.2:c.1209+3661dup	XM_011525375.2:c.1209+3660_1209+3661dup	XM_011525375.2:c.1209+3659_1209+3661dup	XM_011525375.2:c.1209+3658_1209+3661dup	XM_011525375.2:c.1209+3657_1209+3661dup	XM_011525375.2:c.1209+3656_1209+3661dup	XM_011525375.2:c.1209+3655_1209+3661dup	XM_011525375.2:c.1209+3661_1209+3662insAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011525375.2:c.1209+3661_1209+3662insAAAAAAAAAAAAAAAAAAAAAAAAAA
USP32 transcript variant X6	XM_011525376.2:c.1230+3661=	XM_011525376.2:c.1230+3652_1230+3661del	XM_011525376.2:c.1230+3655_1230+3661del	XM_011525376.2:c.1230+3656_1230+3661del	XM_011525376.2:c.1230+3657_1230+3661del	XM_011525376.2:c.1230+3658_1230+3661del	XM_011525376.2:c.1230+3660_1230+3661del	XM_011525376.2:c.1230+3661del	XM_011525376.2:c.1230+3661dup	XM_011525376.2:c.1230+3660_1230+3661dup	XM_011525376.2:c.1230+3659_1230+3661dup	XM_011525376.2:c.1230+3658_1230+3661dup	XM_011525376.2:c.1230+3657_1230+3661dup	XM_011525376.2:c.1230+3656_1230+3661dup	XM_011525376.2:c.1230+3655_1230+3661dup	XM_011525376.2:c.1230+3661_1230+3662insAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011525376.2:c.1230+3661_1230+3662insAAAAAAAAAAAAAAAAAAAAAAAAAA
USP32 transcript variant X8	XM_011525378.2:c.1101+3661=	XM_011525378.2:c.1101+3652_1101+3661del	XM_011525378.2:c.1101+3655_1101+3661del	XM_011525378.2:c.1101+3656_1101+3661del	XM_011525378.2:c.1101+3657_1101+3661del	XM_011525378.2:c.1101+3658_1101+3661del	XM_011525378.2:c.1101+3660_1101+3661del	XM_011525378.2:c.1101+3661del	XM_011525378.2:c.1101+3661dup	XM_011525378.2:c.1101+3660_1101+3661dup	XM_011525378.2:c.1101+3659_1101+3661dup	XM_011525378.2:c.1101+3658_1101+3661dup	XM_011525378.2:c.1101+3657_1101+3661dup	XM_011525378.2:c.1101+3656_1101+3661dup	XM_011525378.2:c.1101+3655_1101+3661dup	XM_011525378.2:c.1101+3661_1101+3662insAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011525378.2:c.1101+3661_1101+3662insAAAAAAAAAAAAAAAAAAAAAAAAAA
USP32 transcript variant X11	XM_011525379.4:c.366+3661=	XM_011525379.4:c.366+3652_366+3661del	XM_011525379.4:c.366+3655_366+3661del	XM_011525379.4:c.366+3656_366+3661del	XM_011525379.4:c.366+3657_366+3661del	XM_011525379.4:c.366+3658_366+3661del	XM_011525379.4:c.366+3660_366+3661del	XM_011525379.4:c.366+3661del	XM_011525379.4:c.366+3661dup	XM_011525379.4:c.366+3660_366+3661dup	XM_011525379.4:c.366+3659_366+3661dup	XM_011525379.4:c.366+3658_366+3661dup	XM_011525379.4:c.366+3657_366+3661dup	XM_011525379.4:c.366+3656_366+3661dup	XM_011525379.4:c.366+3655_366+3661dup	XM_011525379.4:c.366+3661_366+3662insAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011525379.4:c.366+3661_366+3662insAAAAAAAAAAAAAAAAAAAAAAAAAA
USP32 transcript variant X9	XM_017025233.2:c.1101+3661=	XM_017025233.2:c.1101+3652_1101+3661del	XM_017025233.2:c.1101+3655_1101+3661del	XM_017025233.2:c.1101+3656_1101+3661del	XM_017025233.2:c.1101+3657_1101+3661del	XM_017025233.2:c.1101+3658_1101+3661del	XM_017025233.2:c.1101+3660_1101+3661del	XM_017025233.2:c.1101+3661del	XM_017025233.2:c.1101+3661dup	XM_017025233.2:c.1101+3660_1101+3661dup	XM_017025233.2:c.1101+3659_1101+3661dup	XM_017025233.2:c.1101+3658_1101+3661dup	XM_017025233.2:c.1101+3657_1101+3661dup	XM_017025233.2:c.1101+3656_1101+3661dup	XM_017025233.2:c.1101+3655_1101+3661dup	XM_017025233.2:c.1101+3661_1101+3662insAAAAAAAAAAAAAAAAAAAAAAAAA	XM_017025233.2:c.1101+3661_1101+3662insAAAAAAAAAAAAAAAAAAAAAAAAAA
USP32 transcript variant X7	XM_047436943.1:c.1209+3661=	XM_047436943.1:c.1209+3652_1209+3661del	XM_047436943.1:c.1209+3655_1209+3661del	XM_047436943.1:c.1209+3656_1209+3661del	XM_047436943.1:c.1209+3657_1209+3661del	XM_047436943.1:c.1209+3658_1209+3661del	XM_047436943.1:c.1209+3660_1209+3661del	XM_047436943.1:c.1209+3661del	XM_047436943.1:c.1209+3661dup	XM_047436943.1:c.1209+3660_1209+3661dup	XM_047436943.1:c.1209+3659_1209+3661dup	XM_047436943.1:c.1209+3658_1209+3661dup	XM_047436943.1:c.1209+3657_1209+3661dup	XM_047436943.1:c.1209+3656_1209+3661dup	XM_047436943.1:c.1209+3655_1209+3661dup	XM_047436943.1:c.1209+3661_1209+3662insAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047436943.1:c.1209+3661_1209+3662insAAAAAAAAAAAAAAAAAAAAAAAAAA
USP32 transcript variant X10	XM_047436944.1:c.894+3661=	XM_047436944.1:c.894+3652_894+3661del	XM_047436944.1:c.894+3655_894+3661del	XM_047436944.1:c.894+3656_894+3661del	XM_047436944.1:c.894+3657_894+3661del	XM_047436944.1:c.894+3658_894+3661del	XM_047436944.1:c.894+3660_894+3661del	XM_047436944.1:c.894+3661del	XM_047436944.1:c.894+3661dup	XM_047436944.1:c.894+3660_894+3661dup	XM_047436944.1:c.894+3659_894+3661dup	XM_047436944.1:c.894+3658_894+3661dup	XM_047436944.1:c.894+3657_894+3661dup	XM_047436944.1:c.894+3656_894+3661dup	XM_047436944.1:c.894+3655_894+3661dup	XM_047436944.1:c.894+3661_894+3662insAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047436944.1:c.894+3661_894+3662insAAAAAAAAAAAAAAAAAAAAAAAAAA
USP32 transcript variant X12	XM_047436945.1:c.324+3661=	XM_047436945.1:c.324+3652_324+3661del	XM_047436945.1:c.324+3655_324+3661del	XM_047436945.1:c.324+3656_324+3661del	XM_047436945.1:c.324+3657_324+3661del	XM_047436945.1:c.324+3658_324+3661del	XM_047436945.1:c.324+3660_324+3661del	XM_047436945.1:c.324+3661del	XM_047436945.1:c.324+3661dup	XM_047436945.1:c.324+3660_324+3661dup	XM_047436945.1:c.324+3659_324+3661dup	XM_047436945.1:c.324+3658_324+3661dup	XM_047436945.1:c.324+3657_324+3661dup	XM_047436945.1:c.324+3656_324+3661dup	XM_047436945.1:c.324+3655_324+3661dup	XM_047436945.1:c.324+3661_324+3662insAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047436945.1:c.324+3661_324+3662insAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

35 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40841090	Oct 12, 2018 (152)
2	HGSV	ss83442598	Oct 12, 2018 (152)
3	EVA_GENOME_DK	ss1575069363	Apr 01, 2015 (144)
4	SWEGEN	ss3015731959	Nov 08, 2017 (151)
5	EVA	ss3834925730	Apr 27, 2020 (154)
6	KRGDB	ss3935732656	Apr 27, 2020 (154)
7	GNOMAD	ss4313735158	Apr 27, 2021 (155)
8	GNOMAD	ss4313735159	Apr 27, 2021 (155)
9	GNOMAD	ss4313735160	Apr 27, 2021 (155)
10	GNOMAD	ss4313735161	Apr 27, 2021 (155)
11	GNOMAD	ss4313735162	Apr 27, 2021 (155)
12	GNOMAD	ss4313735164	Apr 27, 2021 (155)
13	GNOMAD	ss4313735165	Apr 27, 2021 (155)
14	GNOMAD	ss4313735166	Apr 27, 2021 (155)
15	GNOMAD	ss4313735167	Apr 27, 2021 (155)
16	GNOMAD	ss4313735168	Apr 27, 2021 (155)
17	TOPMED	ss5040164042	Apr 27, 2021 (155)
18	TOPMED	ss5040164043	Apr 27, 2021 (155)
19	TOPMED	ss5040164044	Apr 27, 2021 (155)
20	TOMMO_GENOMICS	ss5222982084	Apr 27, 2021 (155)
21	TOMMO_GENOMICS	ss5222982085	Apr 27, 2021 (155)
22	TOMMO_GENOMICS	ss5222982086	Apr 27, 2021 (155)
23	1000G_HIGH_COVERAGE	ss5303552776	Oct 16, 2022 (156)
24	1000G_HIGH_COVERAGE	ss5303552777	Oct 16, 2022 (156)
25	1000G_HIGH_COVERAGE	ss5303552778	Oct 16, 2022 (156)
26	HUGCELL_USP	ss5496556358	Oct 16, 2022 (156)
27	HUGCELL_USP	ss5496556359	Oct 16, 2022 (156)
28	HUGCELL_USP	ss5496556360	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5496556361	Oct 16, 2022 (156)
30	TOMMO_GENOMICS	ss5779367605	Oct 16, 2022 (156)
31	TOMMO_GENOMICS	ss5779367606	Oct 16, 2022 (156)
32	TOMMO_GENOMICS	ss5779367607	Oct 16, 2022 (156)
33	TOMMO_GENOMICS	ss5779367608	Oct 16, 2022 (156)
34	TOMMO_GENOMICS	ss5779367609	Oct 16, 2022 (156)
35	EVA	ss5851852760	Oct 16, 2022 (156)
36	The Danish reference pan genome	NC_000017.10 - 58309838	Apr 27, 2020 (154)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510774184 (NC_000017.11:60232476::T 16736/109574) Row 510774185 (NC_000017.11:60232476::TT 383/109642) Row 510774186 (NC_000017.11:60232476::TTTT 1/109646)...	-	Apr 27, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510774184 (NC_000017.11:60232476::T 16736/109574) Row 510774185 (NC_000017.11:60232476::TT 383/109642) Row 510774186 (NC_000017.11:60232476::TTTT 1/109646)...	-	Apr 27, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510774184 (NC_000017.11:60232476::T 16736/109574) Row 510774185 (NC_000017.11:60232476::TT 383/109642) Row 510774186 (NC_000017.11:60232476::TTTT 1/109646)...	-	Apr 27, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510774184 (NC_000017.11:60232476::T 16736/109574) Row 510774185 (NC_000017.11:60232476::TT 383/109642) Row 510774186 (NC_000017.11:60232476::TTTT 1/109646)...	-	Apr 27, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510774184 (NC_000017.11:60232476::T 16736/109574) Row 510774185 (NC_000017.11:60232476::TT 383/109642) Row 510774186 (NC_000017.11:60232476::TTTT 1/109646)...	-	Apr 27, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510774184 (NC_000017.11:60232476::T 16736/109574) Row 510774185 (NC_000017.11:60232476::TT 383/109642) Row 510774186 (NC_000017.11:60232476::TTTT 1/109646)...	-	Apr 27, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510774184 (NC_000017.11:60232476::T 16736/109574) Row 510774185 (NC_000017.11:60232476::TT 383/109642) Row 510774186 (NC_000017.11:60232476::TTTT 1/109646)...	-	Apr 27, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510774184 (NC_000017.11:60232476::T 16736/109574) Row 510774185 (NC_000017.11:60232476::TT 383/109642) Row 510774186 (NC_000017.11:60232476::TTTT 1/109646)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510774184 (NC_000017.11:60232476::T 16736/109574) Row 510774185 (NC_000017.11:60232476::TT 383/109642) Row 510774186 (NC_000017.11:60232476::TTTT 1/109646)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510774184 (NC_000017.11:60232476::T 16736/109574) Row 510774185 (NC_000017.11:60232476::TT 383/109642) Row 510774186 (NC_000017.11:60232476::TTTT 1/109646)...	-	Apr 27, 2021 (155)
47	KOREAN population from KRGDB	NC_000017.10 - 58309838	Apr 27, 2020 (154)
48	8.3KJPN Submission ignored due to conflicting rows: Row 80951391 (NC_000017.10:58309837::T 1125/16750) Row 80951392 (NC_000017.10:58309837:T: 135/16750) Row 80951393 (NC_000017.10:58309837::TTTTTTTTTTTTTTTTTTTTTTTTT 13/16750)	-	Apr 27, 2021 (155)
49	8.3KJPN Submission ignored due to conflicting rows: Row 80951391 (NC_000017.10:58309837::T 1125/16750) Row 80951392 (NC_000017.10:58309837:T: 135/16750) Row 80951393 (NC_000017.10:58309837::TTTTTTTTTTTTTTTTTTTTTTTTT 13/16750)	-	Apr 27, 2021 (155)
50	8.3KJPN Submission ignored due to conflicting rows: Row 80951391 (NC_000017.10:58309837::T 1125/16750) Row 80951392 (NC_000017.10:58309837:T: 135/16750) Row 80951393 (NC_000017.10:58309837::TTTTTTTTTTTTTTTTTTTTTTTTT 13/16750)	-	Apr 27, 2021 (155)
51	14KJPN Submission ignored due to conflicting rows: Row 113204709 (NC_000017.11:60232476::T 1901/28238) Row 113204710 (NC_000017.11:60232476:T: 201/28238) Row 113204711 (NC_000017.11:60232476::TT 4/28238)...	-	Oct 16, 2022 (156)
52	14KJPN Submission ignored due to conflicting rows: Row 113204709 (NC_000017.11:60232476::T 1901/28238) Row 113204710 (NC_000017.11:60232476:T: 201/28238) Row 113204711 (NC_000017.11:60232476::TT 4/28238)...	-	Oct 16, 2022 (156)
53	14KJPN Submission ignored due to conflicting rows: Row 113204709 (NC_000017.11:60232476::T 1901/28238) Row 113204710 (NC_000017.11:60232476:T: 201/28238) Row 113204711 (NC_000017.11:60232476::TT 4/28238)...	-	Oct 16, 2022 (156)
54	14KJPN Submission ignored due to conflicting rows: Row 113204709 (NC_000017.11:60232476::T 1901/28238) Row 113204710 (NC_000017.11:60232476:T: 201/28238) Row 113204711 (NC_000017.11:60232476::TT 4/28238)...	-	Oct 16, 2022 (156)
55	14KJPN Submission ignored due to conflicting rows: Row 113204709 (NC_000017.11:60232476::T 1901/28238) Row 113204710 (NC_000017.11:60232476:T: 201/28238) Row 113204711 (NC_000017.11:60232476::TT 4/28238)...	-	Oct 16, 2022 (156)
56	TopMed Submission ignored due to conflicting rows: Row 255709704 (NC_000017.11:60232476::TTTTT 1/264690) Row 255709705 (NC_000017.11:60232476:TTTTTTT: 13/264690) Row 255709706 (NC_000017.11:60232476:TTTTTTTTTT: 4/264690)	-	Apr 27, 2021 (155)
57	TopMed Submission ignored due to conflicting rows: Row 255709704 (NC_000017.11:60232476::TTTTT 1/264690) Row 255709705 (NC_000017.11:60232476:TTTTTTT: 13/264690) Row 255709706 (NC_000017.11:60232476:TTTTTTTTTT: 4/264690)	-	Apr 27, 2021 (155)
58	TopMed Submission ignored due to conflicting rows: Row 255709704 (NC_000017.11:60232476::TTTTT 1/264690) Row 255709705 (NC_000017.11:60232476:TTTTTTT: 13/264690) Row 255709706 (NC_000017.11:60232476:TTTTTTTTTT: 4/264690)	-	Apr 27, 2021 (155)
59	ALFA	NC_000017.11 - 60232477	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
ss5040164044	NC_000017.11:60232476:TTTTTTTTTT:	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
6849613127	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4313735168, ss5040164043	NC_000017.11:60232476:TTTTTTT:	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
6849613127	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4313735167	NC_000017.11:60232476:TTTTTT:	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
6849613127	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
6849613127	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4313735166	NC_000017.11:60232476:TTTT:	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4313735165, ss5496556361	NC_000017.11:60232476:TT:	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
6849613127	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
569394, ss1575069363, ss3015731959, ss5222982085	NC_000017.10:58309837:T:	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4313735164, ss5303552778, ss5496556358, ss5779367606, ss5851852760	NC_000017.11:60232476:T:	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
6849613127	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
42910050, ss3834925730, ss3935732656, ss5222982084	NC_000017.10:58309837::T	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4313735158, ss5303552776, ss5496556359, ss5779367605	NC_000017.11:60232476::T	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
6849613127	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss40841090	NT_010783.15:23583989::T	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss83442598	NT_010783.15:23584009::T	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4313735159, ss5303552777, ss5496556360, ss5779367607	NC_000017.11:60232476::TT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
6849613127	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
6849613127	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4313735160	NC_000017.11:60232476::TTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
6849613127	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5040164042	NC_000017.11:60232476::TTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6849613127	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4313735161	NC_000017.11:60232476::TTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6849613127	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4313735162	NC_000017.11:60232476::TTTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6849613127	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5222982086	NC_000017.10:58309837::TTTTTTTTTTT… NC_000017.10:58309837::TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5779367608	NC_000017.11:60232476::TTTTTTTTTTT… NC_000017.11:60232476::TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ss5779367609	NC_000017.11:60232476::TTTTTTTTTTT… NC_000017.11:60232476::TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2382968269	NC_000017.10:58309837:TTTTTTT:	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT
ss3266015623	NC_000017.11:60232476::TTT	NC_000017.11:60232476:TTTTTTTTTTTT… NC_000017.11:60232476:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT

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

No publications for rs764051983

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

rs764051983