Name: rs10657323
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.

rs10657323

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:658666-658679 (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)₇ / del(T)₆ / del(T)₅ / del(…
del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.1660 (1417/8537, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: EXOC2 : Intron Variant
HUS1B : 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	8537	TTTTTTTTTTTTTT=0.7766	TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0025, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0076, TTTTTTTTTTTTTTT=0.1660, TTTTTTTTTTTTTTTT=0.0473, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000	0.7628	0.090909	0.14629	32
European	Sub	6245	TTTTTTTTTTTTTT=0.6950	TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0034, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0104, TTTTTTTTTTTTTTT=0.2266, TTTTTTTTTTTTTTTT=0.0647, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000	0.662192	0.129754	0.208054	32
African	Sub	1732	TTTTTTTTTTTTTT=1.0000	TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	78	TTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1654	TTTTTTTTTTTTTT=1.0000	TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	14	TTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	6	TTTTTTTTTTTTTT=1.0	TTTTTTT=0.0, TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	8	TTTTTTTTTTTTTT=1.0	TTTTTTT=0.0, TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	70	TTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	228	TTTTTTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	48	TTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	200	TTTTTTTTTTTTTT=0.990	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.010, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	0.98	0.0	0.02	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	8537	(T)₁₄=0.7766	del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0025, delTT=0.0000, delT=0.0076, dupT=0.1660, dupTT=0.0473, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	European	Sub	6245	(T)₁₄=0.6950	del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0034, delTT=0.0000, delT=0.0104, dupT=0.2266, dupTT=0.0647, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	African	Sub	1732	(T)₁₄=1.0000	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
Allele Frequency Aggregator	Latin American 2	Sub	228	(T)₁₄=1.000	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
Allele Frequency Aggregator	Other	Sub	200	(T)₁₄=0.990	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=0.010, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	70	(T)₁₄=1.00	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
Allele Frequency Aggregator	South Asian	Sub	48	(T)₁₄=1.00	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
Allele Frequency Aggregator	Asian	Sub	14	(T)₁₄=1.00	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

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 6	NC_000006.12:g.658673_658679del
GRCh38.p14 chr 6	NC_000006.12:g.658674_658679del
GRCh38.p14 chr 6	NC_000006.12:g.658675_658679del
GRCh38.p14 chr 6	NC_000006.12:g.658676_658679del
GRCh38.p14 chr 6	NC_000006.12:g.658677_658679del
GRCh38.p14 chr 6	NC_000006.12:g.658678_658679del
GRCh38.p14 chr 6	NC_000006.12:g.658679del
GRCh38.p14 chr 6	NC_000006.12:g.658679dup
GRCh38.p14 chr 6	NC_000006.12:g.658678_658679dup
GRCh38.p14 chr 6	NC_000006.12:g.658677_658679dup
GRCh38.p14 chr 6	NC_000006.12:g.658676_658679dup
GRCh37.p13 chr 6	NC_000006.11:g.658673_658679del
GRCh37.p13 chr 6	NC_000006.11:g.658674_658679del
GRCh37.p13 chr 6	NC_000006.11:g.658675_658679del
GRCh37.p13 chr 6	NC_000006.11:g.658676_658679del
GRCh37.p13 chr 6	NC_000006.11:g.658677_658679del
GRCh37.p13 chr 6	NC_000006.11:g.658678_658679del
GRCh37.p13 chr 6	NC_000006.11:g.658679del
GRCh37.p13 chr 6	NC_000006.11:g.658679dup
GRCh37.p13 chr 6	NC_000006.11:g.658678_658679dup
GRCh37.p13 chr 6	NC_000006.11:g.658677_658679dup
GRCh37.p13 chr 6	NC_000006.11:g.658676_658679dup
EXOC2 RefSeqGene	NG_047166.1:g.39470_39476del
EXOC2 RefSeqGene	NG_047166.1:g.39471_39476del
EXOC2 RefSeqGene	NG_047166.1:g.39472_39476del
EXOC2 RefSeqGene	NG_047166.1:g.39473_39476del
EXOC2 RefSeqGene	NG_047166.1:g.39474_39476del
EXOC2 RefSeqGene	NG_047166.1:g.39475_39476del
EXOC2 RefSeqGene	NG_047166.1:g.39476del
EXOC2 RefSeqGene	NG_047166.1:g.39476dup
EXOC2 RefSeqGene	NG_047166.1:g.39475_39476dup
EXOC2 RefSeqGene	NG_047166.1:g.39474_39476dup
EXOC2 RefSeqGene	NG_047166.1:g.39473_39476dup

Gene: EXOC2, exocyst complex component 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
EXOC2 transcript variant 1	NM_018303.6:c.-43-20811_-… NM_018303.6:c.-43-20811_-43-20805del	N/A	Intron Variant
EXOC2 transcript variant 2	NR_073064.2:n.	N/A	Intron Variant
EXOC2 transcript variant X1	XM_017011022.2:c.-43-2081… XM_017011022.2:c.-43-20811_-43-20805del	N/A	Intron Variant
EXOC2 transcript variant X3	XM_017011023.2:c.-43-2081… XM_017011023.2:c.-43-20811_-43-20805del	N/A	Intron Variant
EXOC2 transcript variant X4	XM_017011024.2:c.-43-2081… XM_017011024.2:c.-43-20811_-43-20805del	N/A	Intron Variant
EXOC2 transcript variant X13	XM_017011025.2:c.-43-2081… XM_017011025.2:c.-43-20811_-43-20805del	N/A	Intron Variant
EXOC2 transcript variant X16	XM_017011026.2:c.-43-2081… XM_017011026.2:c.-43-20811_-43-20805del	N/A	Intron Variant
EXOC2 transcript variant X2	XM_047419007.1:c.-131-142… XM_047419007.1:c.-131-1422_-131-1416del	N/A	Intron Variant
EXOC2 transcript variant X5	XM_047419008.1:c.-43-2081… XM_047419008.1:c.-43-20811_-43-20805del	N/A	Intron Variant
EXOC2 transcript variant X6	XM_047419009.1:c.-131-142… XM_047419009.1:c.-131-1422_-131-1416del	N/A	Intron Variant
EXOC2 transcript variant X8	XM_047419010.1:c.-209-110… XM_047419010.1:c.-209-11006_-209-11000del	N/A	Intron Variant
EXOC2 transcript variant X7	XM_047419011.1:c.-43-2081… XM_047419011.1:c.-43-20811_-43-20805del	N/A	Intron Variant
EXOC2 transcript variant X9	XM_047419012.1:c.-43-2081… XM_047419012.1:c.-43-20811_-43-20805del	N/A	Intron Variant
EXOC2 transcript variant X10	XM_047419013.1:c.-131-142… XM_047419013.1:c.-131-1422_-131-1416del	N/A	Intron Variant
EXOC2 transcript variant X11	XM_047419014.1:c.-131-142… XM_047419014.1:c.-131-1422_-131-1416del	N/A	Intron Variant
EXOC2 transcript variant X12	XM_047419015.1:c.-209-110… XM_047419015.1:c.-209-11006_-209-11000del	N/A	Intron Variant
EXOC2 transcript variant X14	XM_047419016.1:c.-43-2081… XM_047419016.1:c.-43-20811_-43-20805del	N/A	Intron Variant
EXOC2 transcript variant X15	XM_047419017.1:c.-131-142… XM_047419017.1:c.-131-1422_-131-1416del	N/A	Intron Variant

Gene: HUS1B, HUS1 checkpoint clamp component B (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
HUS1B transcript	NM_148959.4:c.	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)₁₄=	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄
GRCh38.p14 chr 6	NC_000006.12:g.658666_658679=	NC_000006.12:g.658673_658679del	NC_000006.12:g.658674_658679del	NC_000006.12:g.658675_658679del	NC_000006.12:g.658676_658679del	NC_000006.12:g.658677_658679del	NC_000006.12:g.658678_658679del	NC_000006.12:g.658679del	NC_000006.12:g.658679dup	NC_000006.12:g.658678_658679dup	NC_000006.12:g.658677_658679dup	NC_000006.12:g.658676_658679dup
GRCh37.p13 chr 6	NC_000006.11:g.658666_658679=	NC_000006.11:g.658673_658679del	NC_000006.11:g.658674_658679del	NC_000006.11:g.658675_658679del	NC_000006.11:g.658676_658679del	NC_000006.11:g.658677_658679del	NC_000006.11:g.658678_658679del	NC_000006.11:g.658679del	NC_000006.11:g.658679dup	NC_000006.11:g.658678_658679dup	NC_000006.11:g.658677_658679dup	NC_000006.11:g.658676_658679dup
EXOC2 RefSeqGene	NG_047166.1:g.39463_39476=	NG_047166.1:g.39470_39476del	NG_047166.1:g.39471_39476del	NG_047166.1:g.39472_39476del	NG_047166.1:g.39473_39476del	NG_047166.1:g.39474_39476del	NG_047166.1:g.39475_39476del	NG_047166.1:g.39476del	NG_047166.1:g.39476dup	NG_047166.1:g.39475_39476dup	NG_047166.1:g.39474_39476dup	NG_047166.1:g.39473_39476dup
EXOC2 transcript variant 1	NM_018303.5:c.-43-20805=	NM_018303.5:c.-43-20811_-43-20805del	NM_018303.5:c.-43-20810_-43-20805del	NM_018303.5:c.-43-20809_-43-20805del	NM_018303.5:c.-43-20808_-43-20805del	NM_018303.5:c.-43-20807_-43-20805del	NM_018303.5:c.-43-20806_-43-20805del	NM_018303.5:c.-43-20805del	NM_018303.5:c.-43-20805dup	NM_018303.5:c.-43-20806_-43-20805dup	NM_018303.5:c.-43-20807_-43-20805dup	NM_018303.5:c.-43-20808_-43-20805dup
EXOC2 transcript variant 1	NM_018303.6:c.-43-20805=	NM_018303.6:c.-43-20811_-43-20805del	NM_018303.6:c.-43-20810_-43-20805del	NM_018303.6:c.-43-20809_-43-20805del	NM_018303.6:c.-43-20808_-43-20805del	NM_018303.6:c.-43-20807_-43-20805del	NM_018303.6:c.-43-20806_-43-20805del	NM_018303.6:c.-43-20805del	NM_018303.6:c.-43-20805dup	NM_018303.6:c.-43-20806_-43-20805dup	NM_018303.6:c.-43-20807_-43-20805dup	NM_018303.6:c.-43-20808_-43-20805dup
EXOC2 transcript variant X1	XM_017011022.2:c.-43-20805=	XM_017011022.2:c.-43-20811_-43-20805del	XM_017011022.2:c.-43-20810_-43-20805del	XM_017011022.2:c.-43-20809_-43-20805del	XM_017011022.2:c.-43-20808_-43-20805del	XM_017011022.2:c.-43-20807_-43-20805del	XM_017011022.2:c.-43-20806_-43-20805del	XM_017011022.2:c.-43-20805del	XM_017011022.2:c.-43-20805dup	XM_017011022.2:c.-43-20806_-43-20805dup	XM_017011022.2:c.-43-20807_-43-20805dup	XM_017011022.2:c.-43-20808_-43-20805dup
EXOC2 transcript variant X3	XM_017011023.2:c.-43-20805=	XM_017011023.2:c.-43-20811_-43-20805del	XM_017011023.2:c.-43-20810_-43-20805del	XM_017011023.2:c.-43-20809_-43-20805del	XM_017011023.2:c.-43-20808_-43-20805del	XM_017011023.2:c.-43-20807_-43-20805del	XM_017011023.2:c.-43-20806_-43-20805del	XM_017011023.2:c.-43-20805del	XM_017011023.2:c.-43-20805dup	XM_017011023.2:c.-43-20806_-43-20805dup	XM_017011023.2:c.-43-20807_-43-20805dup	XM_017011023.2:c.-43-20808_-43-20805dup
EXOC2 transcript variant X4	XM_017011024.2:c.-43-20805=	XM_017011024.2:c.-43-20811_-43-20805del	XM_017011024.2:c.-43-20810_-43-20805del	XM_017011024.2:c.-43-20809_-43-20805del	XM_017011024.2:c.-43-20808_-43-20805del	XM_017011024.2:c.-43-20807_-43-20805del	XM_017011024.2:c.-43-20806_-43-20805del	XM_017011024.2:c.-43-20805del	XM_017011024.2:c.-43-20805dup	XM_017011024.2:c.-43-20806_-43-20805dup	XM_017011024.2:c.-43-20807_-43-20805dup	XM_017011024.2:c.-43-20808_-43-20805dup
EXOC2 transcript variant X13	XM_017011025.2:c.-43-20805=	XM_017011025.2:c.-43-20811_-43-20805del	XM_017011025.2:c.-43-20810_-43-20805del	XM_017011025.2:c.-43-20809_-43-20805del	XM_017011025.2:c.-43-20808_-43-20805del	XM_017011025.2:c.-43-20807_-43-20805del	XM_017011025.2:c.-43-20806_-43-20805del	XM_017011025.2:c.-43-20805del	XM_017011025.2:c.-43-20805dup	XM_017011025.2:c.-43-20806_-43-20805dup	XM_017011025.2:c.-43-20807_-43-20805dup	XM_017011025.2:c.-43-20808_-43-20805dup
EXOC2 transcript variant X16	XM_017011026.2:c.-43-20805=	XM_017011026.2:c.-43-20811_-43-20805del	XM_017011026.2:c.-43-20810_-43-20805del	XM_017011026.2:c.-43-20809_-43-20805del	XM_017011026.2:c.-43-20808_-43-20805del	XM_017011026.2:c.-43-20807_-43-20805del	XM_017011026.2:c.-43-20806_-43-20805del	XM_017011026.2:c.-43-20805del	XM_017011026.2:c.-43-20805dup	XM_017011026.2:c.-43-20806_-43-20805dup	XM_017011026.2:c.-43-20807_-43-20805dup	XM_017011026.2:c.-43-20808_-43-20805dup
EXOC2 transcript variant X2	XM_047419007.1:c.-131-1416=	XM_047419007.1:c.-131-1422_-131-1416del	XM_047419007.1:c.-131-1421_-131-1416del	XM_047419007.1:c.-131-1420_-131-1416del	XM_047419007.1:c.-131-1419_-131-1416del	XM_047419007.1:c.-131-1418_-131-1416del	XM_047419007.1:c.-131-1417_-131-1416del	XM_047419007.1:c.-131-1416del	XM_047419007.1:c.-131-1416dup	XM_047419007.1:c.-131-1417_-131-1416dup	XM_047419007.1:c.-131-1418_-131-1416dup	XM_047419007.1:c.-131-1419_-131-1416dup
EXOC2 transcript variant X5	XM_047419008.1:c.-43-20805=	XM_047419008.1:c.-43-20811_-43-20805del	XM_047419008.1:c.-43-20810_-43-20805del	XM_047419008.1:c.-43-20809_-43-20805del	XM_047419008.1:c.-43-20808_-43-20805del	XM_047419008.1:c.-43-20807_-43-20805del	XM_047419008.1:c.-43-20806_-43-20805del	XM_047419008.1:c.-43-20805del	XM_047419008.1:c.-43-20805dup	XM_047419008.1:c.-43-20806_-43-20805dup	XM_047419008.1:c.-43-20807_-43-20805dup	XM_047419008.1:c.-43-20808_-43-20805dup
EXOC2 transcript variant X6	XM_047419009.1:c.-131-1416=	XM_047419009.1:c.-131-1422_-131-1416del	XM_047419009.1:c.-131-1421_-131-1416del	XM_047419009.1:c.-131-1420_-131-1416del	XM_047419009.1:c.-131-1419_-131-1416del	XM_047419009.1:c.-131-1418_-131-1416del	XM_047419009.1:c.-131-1417_-131-1416del	XM_047419009.1:c.-131-1416del	XM_047419009.1:c.-131-1416dup	XM_047419009.1:c.-131-1417_-131-1416dup	XM_047419009.1:c.-131-1418_-131-1416dup	XM_047419009.1:c.-131-1419_-131-1416dup
EXOC2 transcript variant X8	XM_047419010.1:c.-209-11000=	XM_047419010.1:c.-209-11006_-209-11000del	XM_047419010.1:c.-209-11005_-209-11000del	XM_047419010.1:c.-209-11004_-209-11000del	XM_047419010.1:c.-209-11003_-209-11000del	XM_047419010.1:c.-209-11002_-209-11000del	XM_047419010.1:c.-209-11001_-209-11000del	XM_047419010.1:c.-209-11000del	XM_047419010.1:c.-209-11000dup	XM_047419010.1:c.-209-11001_-209-11000dup	XM_047419010.1:c.-209-11002_-209-11000dup	XM_047419010.1:c.-209-11003_-209-11000dup
EXOC2 transcript variant X7	XM_047419011.1:c.-43-20805=	XM_047419011.1:c.-43-20811_-43-20805del	XM_047419011.1:c.-43-20810_-43-20805del	XM_047419011.1:c.-43-20809_-43-20805del	XM_047419011.1:c.-43-20808_-43-20805del	XM_047419011.1:c.-43-20807_-43-20805del	XM_047419011.1:c.-43-20806_-43-20805del	XM_047419011.1:c.-43-20805del	XM_047419011.1:c.-43-20805dup	XM_047419011.1:c.-43-20806_-43-20805dup	XM_047419011.1:c.-43-20807_-43-20805dup	XM_047419011.1:c.-43-20808_-43-20805dup
EXOC2 transcript variant X9	XM_047419012.1:c.-43-20805=	XM_047419012.1:c.-43-20811_-43-20805del	XM_047419012.1:c.-43-20810_-43-20805del	XM_047419012.1:c.-43-20809_-43-20805del	XM_047419012.1:c.-43-20808_-43-20805del	XM_047419012.1:c.-43-20807_-43-20805del	XM_047419012.1:c.-43-20806_-43-20805del	XM_047419012.1:c.-43-20805del	XM_047419012.1:c.-43-20805dup	XM_047419012.1:c.-43-20806_-43-20805dup	XM_047419012.1:c.-43-20807_-43-20805dup	XM_047419012.1:c.-43-20808_-43-20805dup
EXOC2 transcript variant X10	XM_047419013.1:c.-131-1416=	XM_047419013.1:c.-131-1422_-131-1416del	XM_047419013.1:c.-131-1421_-131-1416del	XM_047419013.1:c.-131-1420_-131-1416del	XM_047419013.1:c.-131-1419_-131-1416del	XM_047419013.1:c.-131-1418_-131-1416del	XM_047419013.1:c.-131-1417_-131-1416del	XM_047419013.1:c.-131-1416del	XM_047419013.1:c.-131-1416dup	XM_047419013.1:c.-131-1417_-131-1416dup	XM_047419013.1:c.-131-1418_-131-1416dup	XM_047419013.1:c.-131-1419_-131-1416dup
EXOC2 transcript variant X11	XM_047419014.1:c.-131-1416=	XM_047419014.1:c.-131-1422_-131-1416del	XM_047419014.1:c.-131-1421_-131-1416del	XM_047419014.1:c.-131-1420_-131-1416del	XM_047419014.1:c.-131-1419_-131-1416del	XM_047419014.1:c.-131-1418_-131-1416del	XM_047419014.1:c.-131-1417_-131-1416del	XM_047419014.1:c.-131-1416del	XM_047419014.1:c.-131-1416dup	XM_047419014.1:c.-131-1417_-131-1416dup	XM_047419014.1:c.-131-1418_-131-1416dup	XM_047419014.1:c.-131-1419_-131-1416dup
EXOC2 transcript variant X12	XM_047419015.1:c.-209-11000=	XM_047419015.1:c.-209-11006_-209-11000del	XM_047419015.1:c.-209-11005_-209-11000del	XM_047419015.1:c.-209-11004_-209-11000del	XM_047419015.1:c.-209-11003_-209-11000del	XM_047419015.1:c.-209-11002_-209-11000del	XM_047419015.1:c.-209-11001_-209-11000del	XM_047419015.1:c.-209-11000del	XM_047419015.1:c.-209-11000dup	XM_047419015.1:c.-209-11001_-209-11000dup	XM_047419015.1:c.-209-11002_-209-11000dup	XM_047419015.1:c.-209-11003_-209-11000dup
EXOC2 transcript variant X14	XM_047419016.1:c.-43-20805=	XM_047419016.1:c.-43-20811_-43-20805del	XM_047419016.1:c.-43-20810_-43-20805del	XM_047419016.1:c.-43-20809_-43-20805del	XM_047419016.1:c.-43-20808_-43-20805del	XM_047419016.1:c.-43-20807_-43-20805del	XM_047419016.1:c.-43-20806_-43-20805del	XM_047419016.1:c.-43-20805del	XM_047419016.1:c.-43-20805dup	XM_047419016.1:c.-43-20806_-43-20805dup	XM_047419016.1:c.-43-20807_-43-20805dup	XM_047419016.1:c.-43-20808_-43-20805dup
EXOC2 transcript variant X15	XM_047419017.1:c.-131-1416=	XM_047419017.1:c.-131-1422_-131-1416del	XM_047419017.1:c.-131-1421_-131-1416del	XM_047419017.1:c.-131-1420_-131-1416del	XM_047419017.1:c.-131-1419_-131-1416del	XM_047419017.1:c.-131-1418_-131-1416del	XM_047419017.1:c.-131-1417_-131-1416del	XM_047419017.1:c.-131-1416del	XM_047419017.1:c.-131-1416dup	XM_047419017.1:c.-131-1417_-131-1416dup	XM_047419017.1:c.-131-1418_-131-1416dup	XM_047419017.1:c.-131-1419_-131-1416dup

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#.

37 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss77958228	Dec 06, 2007 (137)
2	MCHAISSO	ss3064188619	Nov 08, 2017 (151)
3	MCHAISSO	ss3065064832	Nov 08, 2017 (151)
4	URBANLAB	ss3648248950	Oct 12, 2018 (152)
5	EVA_DECODE	ss3716418796	Jul 13, 2019 (153)
6	EVA_DECODE	ss3716418800	Jul 13, 2019 (153)
7	ACPOP	ss3733129036	Jul 13, 2019 (153)
8	ACPOP	ss3733129037	Jul 13, 2019 (153)
9	ACPOP	ss3733129038	Jul 13, 2019 (153)
10	ACPOP	ss3733129039	Jul 13, 2019 (153)
11	ACPOP	ss3733129040	Jul 13, 2019 (153)
12	PACBIO	ss3785348565	Jul 13, 2019 (153)
13	PACBIO	ss3785348566	Jul 13, 2019 (153)
14	PACBIO	ss3790717124	Jul 13, 2019 (153)
15	PACBIO	ss3790717125	Jul 13, 2019 (153)
16	PACBIO	ss3795594250	Jul 13, 2019 (153)
17	PACBIO	ss3795594251	Jul 13, 2019 (153)
18	EVA	ss3829686424	Apr 26, 2020 (154)
19	GNOMAD	ss4135578861	Apr 26, 2021 (155)
20	GNOMAD	ss4135578877	Apr 26, 2021 (155)
21	GNOMAD	ss4135578878	Apr 26, 2021 (155)
22	GNOMAD	ss4135578881	Apr 26, 2021 (155)
23	GNOMAD	ss4135578882	Apr 26, 2021 (155)
24	GNOMAD	ss4135578883	Apr 26, 2021 (155)
25	GNOMAD	ss4135578884	Apr 26, 2021 (155)
26	GNOMAD	ss4135578885	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5175795048	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5175795049	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5175795051	Apr 26, 2021 (155)
30	HUGCELL_USP	ss5464933913	Oct 13, 2022 (156)
31	HUGCELL_USP	ss5464933914	Oct 13, 2022 (156)
32	HUGCELL_USP	ss5464933915	Oct 13, 2022 (156)
33	HUGCELL_USP	ss5464933918	Oct 13, 2022 (156)
34	TOMMO_GENOMICS	ss5713355476	Oct 13, 2022 (156)
35	TOMMO_GENOMICS	ss5713355477	Oct 13, 2022 (156)
36	TOMMO_GENOMICS	ss5713355480	Oct 13, 2022 (156)
37	EVA	ss5855166115	Oct 13, 2022 (156)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214829415 (NC_000006.12:658665::T 33075/105838) Row 214829432 (NC_000006.12:658665::TT 7492/105776) Row 214829433 (NC_000006.12:658665::TTT 24/105816)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214829415 (NC_000006.12:658665::T 33075/105838) Row 214829432 (NC_000006.12:658665::TT 7492/105776) Row 214829433 (NC_000006.12:658665::TTT 24/105816)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214829415 (NC_000006.12:658665::T 33075/105838) Row 214829432 (NC_000006.12:658665::TT 7492/105776) Row 214829433 (NC_000006.12:658665::TTT 24/105816)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214829415 (NC_000006.12:658665::T 33075/105838) Row 214829432 (NC_000006.12:658665::TT 7492/105776) Row 214829433 (NC_000006.12:658665::TTT 24/105816)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214829415 (NC_000006.12:658665::T 33075/105838) Row 214829432 (NC_000006.12:658665::TT 7492/105776) Row 214829433 (NC_000006.12:658665::TTT 24/105816)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214829415 (NC_000006.12:658665::T 33075/105838) Row 214829432 (NC_000006.12:658665::TT 7492/105776) Row 214829433 (NC_000006.12:658665::TTT 24/105816)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214829415 (NC_000006.12:658665::T 33075/105838) Row 214829432 (NC_000006.12:658665::TT 7492/105776) Row 214829433 (NC_000006.12:658665::TTT 24/105816)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214829415 (NC_000006.12:658665::T 33075/105838) Row 214829432 (NC_000006.12:658665::TT 7492/105776) Row 214829433 (NC_000006.12:658665::TTT 24/105816)...	-	Apr 26, 2021 (155)
46	Northern Sweden Submission ignored due to conflicting rows: Row 6413901 (NC_000006.11:658665::T 166/562) Row 6413902 (NC_000006.11:658665::TT 71/562) Row 6413903 (NC_000006.11:658665:T: 5/562)...	-	Jul 13, 2019 (153)
47	Northern Sweden Submission ignored due to conflicting rows: Row 6413901 (NC_000006.11:658665::T 166/562) Row 6413902 (NC_000006.11:658665::TT 71/562) Row 6413903 (NC_000006.11:658665:T: 5/562)...	-	Jul 13, 2019 (153)
48	Northern Sweden Submission ignored due to conflicting rows: Row 6413901 (NC_000006.11:658665::T 166/562) Row 6413902 (NC_000006.11:658665::TT 71/562) Row 6413903 (NC_000006.11:658665:T: 5/562)...	-	Jul 13, 2019 (153)
49	Northern Sweden Submission ignored due to conflicting rows: Row 6413901 (NC_000006.11:658665::T 166/562) Row 6413902 (NC_000006.11:658665::TT 71/562) Row 6413903 (NC_000006.11:658665:T: 5/562)...	-	Jul 13, 2019 (153)
50	Northern Sweden Submission ignored due to conflicting rows: Row 6413901 (NC_000006.11:658665::T 166/562) Row 6413902 (NC_000006.11:658665::TT 71/562) Row 6413903 (NC_000006.11:658665:T: 5/562)...	-	Jul 13, 2019 (153)
51	8.3KJPN Submission ignored due to conflicting rows: Row 33764355 (NC_000006.11:658665:T: 39/16756) Row 33764356 (NC_000006.11:658665::T 8452/16756) Row 33764358 (NC_000006.11:658665::TT 42/16756)	-	Apr 26, 2021 (155)
52	8.3KJPN Submission ignored due to conflicting rows: Row 33764355 (NC_000006.11:658665:T: 39/16756) Row 33764356 (NC_000006.11:658665::T 8452/16756) Row 33764358 (NC_000006.11:658665::TT 42/16756)	-	Apr 26, 2021 (155)
53	8.3KJPN Submission ignored due to conflicting rows: Row 33764355 (NC_000006.11:658665:T: 39/16756) Row 33764356 (NC_000006.11:658665::T 8452/16756) Row 33764358 (NC_000006.11:658665::TT 42/16756)	-	Apr 26, 2021 (155)
54	14KJPN Submission ignored due to conflicting rows: Row 47192580 (NC_000006.12:658665:T: 58/28258) Row 47192581 (NC_000006.12:658665::T 14556/28258) Row 47192584 (NC_000006.12:658665::TT 78/28258)	-	Oct 13, 2022 (156)
55	14KJPN Submission ignored due to conflicting rows: Row 47192580 (NC_000006.12:658665:T: 58/28258) Row 47192581 (NC_000006.12:658665::T 14556/28258) Row 47192584 (NC_000006.12:658665::TT 78/28258)	-	Oct 13, 2022 (156)
56	14KJPN Submission ignored due to conflicting rows: Row 47192580 (NC_000006.12:658665:T: 58/28258) Row 47192581 (NC_000006.12:658665::T 14556/28258) Row 47192584 (NC_000006.12:658665::TT 78/28258)	-	Oct 13, 2022 (156)
57	ALFA	NC_000006.12 - 658666	Apr 26, 2021 (155)

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

Associated ID	History Updated (Build)
rs11426531	Jul 30, 2012 (137)
rs55885560	May 11, 2012 (137)
rs60006145	May 23, 2008 (130)
rs72039187	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
6573367764	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTT	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTT	(self)
6573367764	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTT	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTT	(self)
ss4135578885	NC_000006.12:658665:TTTTT:	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTT	(self)
6573367764	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTT	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4135578884, ss5464933918	NC_000006.12:658665:TTTT:	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTT	(self)
6573367764	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTT	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss3733129039	NC_000006.11:658665:TTT:	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4135578883	NC_000006.12:658665:TTT:	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
6573367764	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3733129040	NC_000006.11:658665:TT:	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4135578882	NC_000006.12:658665:TT:	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
6573367764	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3733129038, ss5175795048	NC_000006.11:658665:T:	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3716418796, ss4135578881, ss5464933913, ss5713355476	NC_000006.12:658665:T:	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
6573367764	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3733129036, ss3785348566, ss3790717124, ss3795594250, ss5175795049	NC_000006.11:658665::T	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3064188619, ss3065064832, ss4135578861, ss5464933915, ss5713355477, ss5855166115	NC_000006.12:658665::T	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
6573367764	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3733129037, ss3785348565, ss3790717125, ss3795594251, ss3829686424, ss5175795051	NC_000006.11:658665::TT	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3648248950, ss4135578877, ss5464933914, ss5713355480	NC_000006.12:658665::TT	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
6573367764	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3716418800	NC_000006.12:658666::TT	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss77958228	NT_007592.15:598679::TT	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4135578878	NC_000006.12:658665::TTT	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
6573367764	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
6573367764	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3488103004	NC_000006.12:658665::TTTT	NC_000006.12:658665:TTTTTTTTTTTTTT… NC_000006.12:658665:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT

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

No publications for rs10657323

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

rs10657323