Name: rs11397922
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.

rs11397922

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:86085454-86085470 (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)₉ / del(T)₇ / del(T)₅ / del(…
del(T)₉ / del(T)₇ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / insTTGAGG(T)₂₄ / dupTTT / insTTTATG(T)₂₅ / insTTTA(T)₂₆ / dup(T)₄ / ins(T)₄AGG(T)₃₀ / dup(T)₅ / ins(T)₅G(T)₁₈ / ins(T)₅G(T)₂₄ / dup(T)₆ / ins(T)₆G(T)₂₅ / dup(T)₇ / dup(T)₈ / dup(T)₁₁ / ins(T)₃₅A(T)₃₈CATAA(T)₅GCCCTAA(T)₂₅ / ins(T)₄₁ / ins(T)₄₂
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.1429 (1114/7796, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GOLM1 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	7796	TTTTTTTTTTTTTTTTT=0.7926	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.1429, TTTTTTTTTTTTTTTTTTT=0.0540, TTTTTTTTTTTTTTTTTTTTTTTT=0.0068, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0028, TTTTTTTTTTTTTTTTTTTT=0.0009, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	0.800702	0.080773	0.118525	32
European	Sub	5846	TTTTTTTTTTTTTTTTT=0.7237	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.1902, TTTTTTTTTTTTTTTTTTT=0.0720, TTTTTTTTTTTTTTTTTTTTTTTT=0.0091, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0038, TTTTTTTTTTTTTTTTTTTT=0.0012, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	0.721949	0.113022	0.165029	32
African	Sub	1314	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	50	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1264	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	98	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	76	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	22	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	44	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	274	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	46	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	174	TTTTTTTTTTTTTTTTT=0.989	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.011, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	0.977011	0.0	0.022989	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	7796	(T)₁₇=0.7926	del(T)₉=0.0000, del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.1429, dupTT=0.0540, dupTTT=0.0009, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₇=0.0068, dup(T)₈=0.0028
Allele Frequency Aggregator	European	Sub	5846	(T)₁₇=0.7237	del(T)₉=0.0000, del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.1902, dupTT=0.0720, dupTTT=0.0012, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₇=0.0091, dup(T)₈=0.0038
Allele Frequency Aggregator	African	Sub	1314	(T)₁₇=1.0000	del(T)₉=0.0000, del(T)₇=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)₇=0.0000, dup(T)₈=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	274	(T)₁₇=1.000	del(T)₉=0.000, del(T)₇=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)₇=0.000, dup(T)₈=0.000
Allele Frequency Aggregator	Other	Sub	174	(T)₁₇=0.989	del(T)₉=0.000, del(T)₇=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.011, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₇=0.000, dup(T)₈=0.000
Allele Frequency Aggregator	Asian	Sub	98	(T)₁₇=1.00	del(T)₉=0.00, del(T)₇=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)₇=0.00, dup(T)₈=0.00
Allele Frequency Aggregator	South Asian	Sub	46	(T)₁₇=1.00	del(T)₉=0.00, del(T)₇=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)₇=0.00, dup(T)₈=0.00
Allele Frequency Aggregator	Latin American 1	Sub	44	(T)₁₇=1.00	del(T)₉=0.00, del(T)₇=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)₇=0.00, dup(T)₈=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 9	NC_000009.12:g.86085462_86085470del
GRCh38.p14 chr 9	NC_000009.12:g.86085464_86085470del
GRCh38.p14 chr 9	NC_000009.12:g.86085466_86085470del
GRCh38.p14 chr 9	NC_000009.12:g.86085467_86085470del
GRCh38.p14 chr 9	NC_000009.12:g.86085468_86085470del
GRCh38.p14 chr 9	NC_000009.12:g.86085469_86085470del
GRCh38.p14 chr 9	NC_000009.12:g.86085470del
GRCh38.p14 chr 9	NC_000009.12:g.86085470dup
GRCh38.p14 chr 9	NC_000009.12:g.86085469_86085470dup
GRCh38.p14 chr 9	NC_000009.12:g.86085454_86085470T[19]GAGGTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 9	NC_000009.12:g.86085468_86085470dup
GRCh38.p14 chr 9	NC_000009.12:g.86085454_86085470T[20]ATGTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 9	NC_000009.12:g.86085454_86085470T[20]ATTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 9	NC_000009.12:g.86085467_86085470dup
GRCh38.p14 chr 9	NC_000009.12:g.86085454_86085470T[21]AGGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 9	NC_000009.12:g.86085466_86085470dup
GRCh38.p14 chr 9	NC_000009.12:g.86085454_86085470T[22]GTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 9	NC_000009.12:g.86085454_86085470T[22]GTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 9	NC_000009.12:g.86085465_86085470dup
GRCh38.p14 chr 9	NC_000009.12:g.86085454_86085470T[23]GTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 9	NC_000009.12:g.86085464_86085470dup
GRCh38.p14 chr 9	NC_000009.12:g.86085463_86085470dup
GRCh38.p14 chr 9	NC_000009.12:g.86085460_86085470dup
GRCh38.p14 chr 9	NC_000009.12:g.86085454_86085470T[52]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCATAATTTTTGCCCTAATTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 9	NC_000009.12:g.86085470_86085471insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 9	NC_000009.12:g.86085470_86085471insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 9	NC_000009.11:g.88700377_88700385del
GRCh37.p13 chr 9	NC_000009.11:g.88700379_88700385del
GRCh37.p13 chr 9	NC_000009.11:g.88700381_88700385del
GRCh37.p13 chr 9	NC_000009.11:g.88700382_88700385del
GRCh37.p13 chr 9	NC_000009.11:g.88700383_88700385del
GRCh37.p13 chr 9	NC_000009.11:g.88700384_88700385del
GRCh37.p13 chr 9	NC_000009.11:g.88700385del
GRCh37.p13 chr 9	NC_000009.11:g.88700385dup
GRCh37.p13 chr 9	NC_000009.11:g.88700384_88700385dup
GRCh37.p13 chr 9	NC_000009.11:g.88700369_88700385T[19]GAGGTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 9	NC_000009.11:g.88700383_88700385dup
GRCh37.p13 chr 9	NC_000009.11:g.88700369_88700385T[20]ATGTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 9	NC_000009.11:g.88700369_88700385T[20]ATTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 9	NC_000009.11:g.88700382_88700385dup
GRCh37.p13 chr 9	NC_000009.11:g.88700369_88700385T[21]AGGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 9	NC_000009.11:g.88700381_88700385dup
GRCh37.p13 chr 9	NC_000009.11:g.88700369_88700385T[22]GTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 9	NC_000009.11:g.88700369_88700385T[22]GTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 9	NC_000009.11:g.88700380_88700385dup
GRCh37.p13 chr 9	NC_000009.11:g.88700369_88700385T[23]GTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 9	NC_000009.11:g.88700379_88700385dup
GRCh37.p13 chr 9	NC_000009.11:g.88700378_88700385dup
GRCh37.p13 chr 9	NC_000009.11:g.88700375_88700385dup
GRCh37.p13 chr 9	NC_000009.11:g.88700369_88700385T[52]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCATAATTTTTGCCCTAATTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 9	NC_000009.11:g.88700385_88700386insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 9	NC_000009.11:g.88700385_88700386insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: GOLM1, golgi membrane protein 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
GOLM1 transcript variant 1	NM_016548.4:c.-21-6121_-2… NM_016548.4:c.-21-6121_-21-6113del	N/A	Intron Variant
GOLM1 transcript variant 2	NM_177937.3:c.-21-6121_-2… NM_177937.3:c.-21-6121_-21-6113del	N/A	Intron 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)₁₇=	del(T)₉	del(T)₇	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	insTTGAGG(T)₂₄	dupTTT	insTTTATG(T)₂₅	insTTTA(T)₂₆	dup(T)₄	ins(T)₄AGG(T)₃₀	dup(T)₅	ins(T)₅G(T)₁₈	ins(T)₅G(T)₂₄	dup(T)₆	ins(T)₆G(T)₂₅	dup(T)₇	dup(T)₈	dup(T)₁₁	ins(T)₃₅A(T)₃₈CATAA(T)₅GCCCTAA(T)₂₅	ins(T)₄₁	ins(T)₄₂
GRCh38.p14 chr 9	NC_000009.12:g.86085454_86085470=	NC_000009.12:g.86085462_86085470del	NC_000009.12:g.86085464_86085470del	NC_000009.12:g.86085466_86085470del	NC_000009.12:g.86085467_86085470del	NC_000009.12:g.86085468_86085470del	NC_000009.12:g.86085469_86085470del	NC_000009.12:g.86085470del	NC_000009.12:g.86085470dup	NC_000009.12:g.86085469_86085470dup	NC_000009.12:g.86085454_86085470T[19]GAGGTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000009.12:g.86085468_86085470dup	NC_000009.12:g.86085454_86085470T[20]ATGTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000009.12:g.86085454_86085470T[20]ATTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000009.12:g.86085467_86085470dup	NC_000009.12:g.86085454_86085470T[21]AGGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000009.12:g.86085466_86085470dup	NC_000009.12:g.86085454_86085470T[22]GTTTTTTTTTTTTTTTTTT[1]	NC_000009.12:g.86085454_86085470T[22]GTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000009.12:g.86085465_86085470dup	NC_000009.12:g.86085454_86085470T[23]GTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000009.12:g.86085464_86085470dup	NC_000009.12:g.86085463_86085470dup	NC_000009.12:g.86085460_86085470dup	NC_000009.12:g.86085454_86085470T[52]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCATAATTTTTGCCCTAATTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000009.12:g.86085470_86085471insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:g.86085470_86085471insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 9	NC_000009.11:g.88700369_88700385=	NC_000009.11:g.88700377_88700385del	NC_000009.11:g.88700379_88700385del	NC_000009.11:g.88700381_88700385del	NC_000009.11:g.88700382_88700385del	NC_000009.11:g.88700383_88700385del	NC_000009.11:g.88700384_88700385del	NC_000009.11:g.88700385del	NC_000009.11:g.88700385dup	NC_000009.11:g.88700384_88700385dup	NC_000009.11:g.88700369_88700385T[19]GAGGTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000009.11:g.88700383_88700385dup	NC_000009.11:g.88700369_88700385T[20]ATGTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000009.11:g.88700369_88700385T[20]ATTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000009.11:g.88700382_88700385dup	NC_000009.11:g.88700369_88700385T[21]AGGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000009.11:g.88700381_88700385dup	NC_000009.11:g.88700369_88700385T[22]GTTTTTTTTTTTTTTTTTT[1]	NC_000009.11:g.88700369_88700385T[22]GTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000009.11:g.88700380_88700385dup	NC_000009.11:g.88700369_88700385T[23]GTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000009.11:g.88700379_88700385dup	NC_000009.11:g.88700378_88700385dup	NC_000009.11:g.88700375_88700385dup	NC_000009.11:g.88700369_88700385T[52]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCATAATTTTTGCCCTAATTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000009.11:g.88700385_88700386insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.11:g.88700385_88700386insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GOLM1 transcript variant 1	NM_016548.3:c.-21-6113=	NM_016548.3:c.-21-6121_-21-6113del	NM_016548.3:c.-21-6119_-21-6113del	NM_016548.3:c.-21-6117_-21-6113del	NM_016548.3:c.-21-6116_-21-6113del	NM_016548.3:c.-21-6115_-21-6113del	NM_016548.3:c.-21-6114_-21-6113del	NM_016548.3:c.-21-6113del	NM_016548.3:c.-21-6113dup	NM_016548.3:c.-21-6114_-21-6113dup	NM_016548.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACCTCAA	NM_016548.3:c.-21-6115_-21-6113dup	NM_016548.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACATAAA	NM_016548.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAATAAA	NM_016548.3:c.-21-6116_-21-6113dup	NM_016548.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACCTAAAA	NM_016548.3:c.-21-6117_-21-6113dup	NM_016548.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAACAAAAA	NM_016548.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACAAAAA	NM_016548.3:c.-21-6118_-21-6113dup	NM_016548.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAA	NM_016548.3:c.-21-6119_-21-6113dup	NM_016548.3:c.-21-6120_-21-6113dup	NM_016548.3:c.-21-6123_-21-6113dup	NM_016548.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAATTAGGGCAAAAATTATGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_016548.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_016548.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GOLM1 transcript variant 1	NM_016548.4:c.-21-6113=	NM_016548.4:c.-21-6121_-21-6113del	NM_016548.4:c.-21-6119_-21-6113del	NM_016548.4:c.-21-6117_-21-6113del	NM_016548.4:c.-21-6116_-21-6113del	NM_016548.4:c.-21-6115_-21-6113del	NM_016548.4:c.-21-6114_-21-6113del	NM_016548.4:c.-21-6113del	NM_016548.4:c.-21-6113dup	NM_016548.4:c.-21-6114_-21-6113dup	NM_016548.4:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACCTCAA	NM_016548.4:c.-21-6115_-21-6113dup	NM_016548.4:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACATAAA	NM_016548.4:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAATAAA	NM_016548.4:c.-21-6116_-21-6113dup	NM_016548.4:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACCTAAAA	NM_016548.4:c.-21-6117_-21-6113dup	NM_016548.4:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAACAAAAA	NM_016548.4:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACAAAAA	NM_016548.4:c.-21-6118_-21-6113dup	NM_016548.4:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAA	NM_016548.4:c.-21-6119_-21-6113dup	NM_016548.4:c.-21-6120_-21-6113dup	NM_016548.4:c.-21-6123_-21-6113dup	NM_016548.4:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAATTAGGGCAAAAATTATGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_016548.4:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_016548.4:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GOLM1 transcript variant 2	NM_177937.2:c.-21-6113=	NM_177937.2:c.-21-6121_-21-6113del	NM_177937.2:c.-21-6119_-21-6113del	NM_177937.2:c.-21-6117_-21-6113del	NM_177937.2:c.-21-6116_-21-6113del	NM_177937.2:c.-21-6115_-21-6113del	NM_177937.2:c.-21-6114_-21-6113del	NM_177937.2:c.-21-6113del	NM_177937.2:c.-21-6113dup	NM_177937.2:c.-21-6114_-21-6113dup	NM_177937.2:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACCTCAA	NM_177937.2:c.-21-6115_-21-6113dup	NM_177937.2:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACATAAA	NM_177937.2:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAATAAA	NM_177937.2:c.-21-6116_-21-6113dup	NM_177937.2:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACCTAAAA	NM_177937.2:c.-21-6117_-21-6113dup	NM_177937.2:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAACAAAAA	NM_177937.2:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACAAAAA	NM_177937.2:c.-21-6118_-21-6113dup	NM_177937.2:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAA	NM_177937.2:c.-21-6119_-21-6113dup	NM_177937.2:c.-21-6120_-21-6113dup	NM_177937.2:c.-21-6123_-21-6113dup	NM_177937.2:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAATTAGGGCAAAAATTATGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_177937.2:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_177937.2:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GOLM1 transcript variant 2	NM_177937.3:c.-21-6113=	NM_177937.3:c.-21-6121_-21-6113del	NM_177937.3:c.-21-6119_-21-6113del	NM_177937.3:c.-21-6117_-21-6113del	NM_177937.3:c.-21-6116_-21-6113del	NM_177937.3:c.-21-6115_-21-6113del	NM_177937.3:c.-21-6114_-21-6113del	NM_177937.3:c.-21-6113del	NM_177937.3:c.-21-6113dup	NM_177937.3:c.-21-6114_-21-6113dup	NM_177937.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACCTCAA	NM_177937.3:c.-21-6115_-21-6113dup	NM_177937.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACATAAA	NM_177937.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAATAAA	NM_177937.3:c.-21-6116_-21-6113dup	NM_177937.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACCTAAAA	NM_177937.3:c.-21-6117_-21-6113dup	NM_177937.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAACAAAAA	NM_177937.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACAAAAA	NM_177937.3:c.-21-6118_-21-6113dup	NM_177937.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAA	NM_177937.3:c.-21-6119_-21-6113dup	NM_177937.3:c.-21-6120_-21-6113dup	NM_177937.3:c.-21-6123_-21-6113dup	NM_177937.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAATTAGGGCAAAAATTATGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_177937.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_177937.3:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GOLM1 transcript variant X1	XM_005252040.1:c.-21-6113=	XM_005252040.1:c.-21-6121_-21-6113del	XM_005252040.1:c.-21-6119_-21-6113del	XM_005252040.1:c.-21-6117_-21-6113del	XM_005252040.1:c.-21-6116_-21-6113del	XM_005252040.1:c.-21-6115_-21-6113del	XM_005252040.1:c.-21-6114_-21-6113del	XM_005252040.1:c.-21-6113del	XM_005252040.1:c.-21-6113dup	XM_005252040.1:c.-21-6114_-21-6113dup	XM_005252040.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACCTCAA	XM_005252040.1:c.-21-6115_-21-6113dup	XM_005252040.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACATAAA	XM_005252040.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAATAAA	XM_005252040.1:c.-21-6116_-21-6113dup	XM_005252040.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACCTAAAA	XM_005252040.1:c.-21-6117_-21-6113dup	XM_005252040.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAACAAAAA	XM_005252040.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACAAAAA	XM_005252040.1:c.-21-6118_-21-6113dup	XM_005252040.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAA	XM_005252040.1:c.-21-6119_-21-6113dup	XM_005252040.1:c.-21-6120_-21-6113dup	XM_005252040.1:c.-21-6123_-21-6113dup	XM_005252040.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAATTAGGGCAAAAATTATGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252040.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252040.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GOLM1 transcript variant X2	XM_005252041.1:c.-21-6113=	XM_005252041.1:c.-21-6121_-21-6113del	XM_005252041.1:c.-21-6119_-21-6113del	XM_005252041.1:c.-21-6117_-21-6113del	XM_005252041.1:c.-21-6116_-21-6113del	XM_005252041.1:c.-21-6115_-21-6113del	XM_005252041.1:c.-21-6114_-21-6113del	XM_005252041.1:c.-21-6113del	XM_005252041.1:c.-21-6113dup	XM_005252041.1:c.-21-6114_-21-6113dup	XM_005252041.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACCTCAA	XM_005252041.1:c.-21-6115_-21-6113dup	XM_005252041.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACATAAA	XM_005252041.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAATAAA	XM_005252041.1:c.-21-6116_-21-6113dup	XM_005252041.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACCTAAAA	XM_005252041.1:c.-21-6117_-21-6113dup	XM_005252041.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAACAAAAA	XM_005252041.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACAAAAA	XM_005252041.1:c.-21-6118_-21-6113dup	XM_005252041.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAA	XM_005252041.1:c.-21-6119_-21-6113dup	XM_005252041.1:c.-21-6120_-21-6113dup	XM_005252041.1:c.-21-6123_-21-6113dup	XM_005252041.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAATTAGGGCAAAAATTATGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252041.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252041.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GOLM1 transcript variant X3	XM_005252042.1:c.-21-6113=	XM_005252042.1:c.-21-6121_-21-6113del	XM_005252042.1:c.-21-6119_-21-6113del	XM_005252042.1:c.-21-6117_-21-6113del	XM_005252042.1:c.-21-6116_-21-6113del	XM_005252042.1:c.-21-6115_-21-6113del	XM_005252042.1:c.-21-6114_-21-6113del	XM_005252042.1:c.-21-6113del	XM_005252042.1:c.-21-6113dup	XM_005252042.1:c.-21-6114_-21-6113dup	XM_005252042.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACCTCAA	XM_005252042.1:c.-21-6115_-21-6113dup	XM_005252042.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACATAAA	XM_005252042.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAATAAA	XM_005252042.1:c.-21-6116_-21-6113dup	XM_005252042.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACCTAAAA	XM_005252042.1:c.-21-6117_-21-6113dup	XM_005252042.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAACAAAAA	XM_005252042.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACAAAAA	XM_005252042.1:c.-21-6118_-21-6113dup	XM_005252042.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAA	XM_005252042.1:c.-21-6119_-21-6113dup	XM_005252042.1:c.-21-6120_-21-6113dup	XM_005252042.1:c.-21-6123_-21-6113dup	XM_005252042.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAATTAGGGCAAAAATTATGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252042.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252042.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GOLM1 transcript variant X4	XM_005252043.1:c.-21-6113=	XM_005252043.1:c.-21-6121_-21-6113del	XM_005252043.1:c.-21-6119_-21-6113del	XM_005252043.1:c.-21-6117_-21-6113del	XM_005252043.1:c.-21-6116_-21-6113del	XM_005252043.1:c.-21-6115_-21-6113del	XM_005252043.1:c.-21-6114_-21-6113del	XM_005252043.1:c.-21-6113del	XM_005252043.1:c.-21-6113dup	XM_005252043.1:c.-21-6114_-21-6113dup	XM_005252043.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACCTCAA	XM_005252043.1:c.-21-6115_-21-6113dup	XM_005252043.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACATAAA	XM_005252043.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAATAAA	XM_005252043.1:c.-21-6116_-21-6113dup	XM_005252043.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACCTAAAA	XM_005252043.1:c.-21-6117_-21-6113dup	XM_005252043.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAACAAAAA	XM_005252043.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACAAAAA	XM_005252043.1:c.-21-6118_-21-6113dup	XM_005252043.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAA	XM_005252043.1:c.-21-6119_-21-6113dup	XM_005252043.1:c.-21-6120_-21-6113dup	XM_005252043.1:c.-21-6123_-21-6113dup	XM_005252043.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAATTAGGGCAAAAATTATGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252043.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252043.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GOLM1 transcript variant X5	XM_005252044.1:c.-21-6113=	XM_005252044.1:c.-21-6121_-21-6113del	XM_005252044.1:c.-21-6119_-21-6113del	XM_005252044.1:c.-21-6117_-21-6113del	XM_005252044.1:c.-21-6116_-21-6113del	XM_005252044.1:c.-21-6115_-21-6113del	XM_005252044.1:c.-21-6114_-21-6113del	XM_005252044.1:c.-21-6113del	XM_005252044.1:c.-21-6113dup	XM_005252044.1:c.-21-6114_-21-6113dup	XM_005252044.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACCTCAA	XM_005252044.1:c.-21-6115_-21-6113dup	XM_005252044.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACATAAA	XM_005252044.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAATAAA	XM_005252044.1:c.-21-6116_-21-6113dup	XM_005252044.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACCTAAAA	XM_005252044.1:c.-21-6117_-21-6113dup	XM_005252044.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAACAAAAA	XM_005252044.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAACAAAAA	XM_005252044.1:c.-21-6118_-21-6113dup	XM_005252044.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAA	XM_005252044.1:c.-21-6119_-21-6113dup	XM_005252044.1:c.-21-6120_-21-6113dup	XM_005252044.1:c.-21-6123_-21-6113dup	XM_005252044.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAATTAGGGCAAAAATTATGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252044.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252044.1:c.-21-6113_-21-6112insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

50 SubSNP, 35 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95519992	Oct 12, 2018 (152)
2	PJP	ss295426471	Oct 12, 2018 (152)
3	BILGI_BIOE	ss666474436	Apr 25, 2013 (138)
4	MCHAISSO	ss3065234452	Nov 08, 2017 (151)
5	EVA	ss3831722485	Apr 26, 2020 (154)
6	GNOMAD	ss4204845770	Apr 26, 2021 (155)
7	GNOMAD	ss4204845771	Apr 26, 2021 (155)
8	GNOMAD	ss4204845774	Apr 26, 2021 (155)
9	GNOMAD	ss4204845775	Apr 26, 2021 (155)
10	GNOMAD	ss4204845776	Apr 26, 2021 (155)
11	GNOMAD	ss4204845777	Apr 26, 2021 (155)
12	GNOMAD	ss4204845778	Apr 26, 2021 (155)
13	GNOMAD	ss4204845779	Apr 26, 2021 (155)
14	GNOMAD	ss4204845780	Apr 26, 2021 (155)
15	GNOMAD	ss4204845781	Apr 26, 2021 (155)
16	GNOMAD	ss4204845782	Apr 26, 2021 (155)
17	GNOMAD	ss4204845783	Apr 26, 2021 (155)
18	GNOMAD	ss4204845784	Apr 26, 2021 (155)
19	GNOMAD	ss4204845785	Apr 26, 2021 (155)
20	GNOMAD	ss4204845786	Apr 26, 2021 (155)
21	GNOMAD	ss4204845787	Apr 26, 2021 (155)
22	GNOMAD	ss4204845788	Apr 26, 2021 (155)
23	GNOMAD	ss4204845790	Apr 26, 2021 (155)
24	GNOMAD	ss4204845791	Apr 26, 2021 (155)
25	GNOMAD	ss4204845792	Apr 26, 2021 (155)
26	GNOMAD	ss4204845793	Apr 26, 2021 (155)
27	GNOMAD	ss4204845794	Apr 26, 2021 (155)
28	GNOMAD	ss4204845795	Apr 26, 2021 (155)
29	GNOMAD	ss4204845796	Apr 26, 2021 (155)
30	TOPMED	ss4826298354	Apr 26, 2021 (155)
31	TOPMED	ss4826298355	Apr 26, 2021 (155)
32	TOPMED	ss4826298356	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5194092140	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5194092141	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5194092142	Apr 26, 2021 (155)
36	1000G_HIGH_COVERAGE	ss5281246230	Oct 13, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5281246231	Oct 13, 2022 (156)
38	HUGCELL_USP	ss5477210632	Oct 13, 2022 (156)
39	HUGCELL_USP	ss5477210633	Oct 13, 2022 (156)
40	HUGCELL_USP	ss5477210634	Oct 13, 2022 (156)
41	HUGCELL_USP	ss5477210635	Oct 13, 2022 (156)
42	HUGCELL_USP	ss5477210636	Oct 13, 2022 (156)
43	TOMMO_GENOMICS	ss5738261014	Oct 13, 2022 (156)
44	TOMMO_GENOMICS	ss5738261015	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5738261016	Oct 13, 2022 (156)
46	YY_MCH	ss5810767115	Oct 13, 2022 (156)
47	EVA	ss5829380192	Oct 13, 2022 (156)
48	EVA	ss5829380193	Oct 13, 2022 (156)
49	EVA	ss5829380194	Oct 13, 2022 (156)
50	EVA	ss5856821151	Oct 13, 2022 (156)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329993468 (NC_000009.12:86085453::T 31191/85354) Row 329993469 (NC_000009.12:86085453::TT 8750/85226) Row 329993472 (NC_000009.12:86085453::TTT 145/85498)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 52061447 (NC_000009.11:88700368::T 1013/15858) Row 52061448 (NC_000009.11:88700368:T: 6/15858) Row 52061449 (NC_000009.11:88700368::TT 8/15858)	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 52061447 (NC_000009.11:88700368::T 1013/15858) Row 52061448 (NC_000009.11:88700368:T: 6/15858) Row 52061449 (NC_000009.11:88700368::TT 8/15858)	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 52061447 (NC_000009.11:88700368::T 1013/15858) Row 52061448 (NC_000009.11:88700368:T: 6/15858) Row 52061449 (NC_000009.11:88700368::TT 8/15858)	-	Apr 26, 2021 (155)
79	14KJPN Submission ignored due to conflicting rows: Row 72098118 (NC_000009.12:86085453::T 1669/28170) Row 72098119 (NC_000009.12:86085453:T: 18/28170) Row 72098120 (NC_000009.12:86085453::TT 18/28170)	-	Oct 13, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 72098118 (NC_000009.12:86085453::T 1669/28170) Row 72098119 (NC_000009.12:86085453:T: 18/28170) Row 72098120 (NC_000009.12:86085453::TT 18/28170)	-	Oct 13, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 72098118 (NC_000009.12:86085453::T 1669/28170) Row 72098119 (NC_000009.12:86085453:T: 18/28170) Row 72098120 (NC_000009.12:86085453::TT 18/28170)	-	Oct 13, 2022 (156)
82	TopMed Submission ignored due to conflicting rows: Row 663675915 (NC_000009.12:86085453:TTTT: 10/264690) Row 663675916 (NC_000009.12:86085453:TTTTT: 2/264690) Row 663675917 (NC_000009.12:86085453:TTTTTTT: 1/264690)	-	Apr 26, 2021 (155)
83	TopMed Submission ignored due to conflicting rows: Row 663675915 (NC_000009.12:86085453:TTTT: 10/264690) Row 663675916 (NC_000009.12:86085453:TTTTT: 2/264690) Row 663675917 (NC_000009.12:86085453:TTTTTTT: 1/264690)	-	Apr 26, 2021 (155)
84	TopMed Submission ignored due to conflicting rows: Row 663675915 (NC_000009.12:86085453:TTTT: 10/264690) Row 663675916 (NC_000009.12:86085453:TTTTT: 2/264690) Row 663675917 (NC_000009.12:86085453:TTTTTTT: 1/264690)	-	Apr 26, 2021 (155)
85	ALFA	NC_000009.12 - 86085454	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4204845796	NC_000009.12:86085453:TTTTTTTTT:	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
6692725812	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
ss4204845795, ss4826298356	NC_000009.12:86085453:TTTTTTT:	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
6692725812	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4204845794, ss4826298355	NC_000009.12:86085453:TTTTT:	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
6692725812	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4204845793, ss4826298354	NC_000009.12:86085453:TTTT:	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
6692725812	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4204845792	NC_000009.12:86085453:TTT:	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
6692725812	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4204845791, ss5477210636	NC_000009.12:86085453:TT:	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
6692725812	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5194092141	NC_000009.11:88700368:T:	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4204845790, ss5281246230, ss5477210633, ss5738261015	NC_000009.12:86085453:T:	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
6692725812	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss295426471	NC_000009.10:87890189::T	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss666474436, ss3831722485, ss5194092140, ss5829380192	NC_000009.11:88700368::T	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3065234452, ss4204845770, ss5281246231, ss5477210632, ss5738261014, ss5810767115	NC_000009.12:86085453::T	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
6692725812	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss95519992	NT_008470.19:17864917::T	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5194092142, ss5829380193	NC_000009.11:88700368::TT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4204845771, ss5477210634, ss5738261016, ss5856821151	NC_000009.12:86085453::TT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
6692725812	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4204845780	NC_000009.12:86085453::TTTTTTTTTTT… NC_000009.12:86085453::TTTTTTTTTTTTTTTTTTTGAGGTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTGAGGTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5829380194	NC_000009.11:88700368::TTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT
ss4204845774, ss5477210635	NC_000009.12:86085453::TTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
6692725812	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4204845781	NC_000009.12:86085453::TTTTTTTTTTT… NC_000009.12:86085453::TTTTTTTTTTTTTTTTTTTTATGTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTATGTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4204845782	NC_000009.12:86085453::TTTTTTTTTTT… NC_000009.12:86085453::TTTTTTTTTTTTTTTTTTTTATTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4204845775	NC_000009.12:86085453::TTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
6692725812	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4204845783	NC_000009.12:86085453::TTTTTTTTTTT… NC_000009.12:86085453::TTTTTTTTTTTTTTTTTTTTTAGGTTTTTTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTAGGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6692725812	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4204845784	NC_000009.12:86085453::TTTTTTTTTTT… NC_000009.12:86085453::TTTTTTTTTTTTTTTTTTTTTTGT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTT	(self)
ss4204845785	NC_000009.12:86085453::TTTTTTTTTTT… NC_000009.12:86085453::TTTTTTTTTTTTTTTTTTTTTTGTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4204845776	NC_000009.12:86085453::TTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4204845786	NC_000009.12:86085453::TTTTTTTTTTT… NC_000009.12:86085453::TTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4204845777	NC_000009.12:86085453::TTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
6692725812	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4204845778	NC_000009.12:86085453::TTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6692725812	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4204845779	NC_000009.12:86085453::TTTTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000009.12:86085453::TTTTTTTTTTT… NC_000009.12:86085453::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCATAATTTTTGCCCTAATTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCATAATTTTTGCCCTAATTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4204845787	NC_000009.12:86085453::TTTTTTTTTTT… NC_000009.12:86085453::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4204845788	NC_000009.12:86085453::TTTTTTTTTTT… NC_000009.12:86085453::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:86085453:TTTTTTTTTTTT… NC_000009.12:86085453:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

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

No publications for rs11397922

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

rs11397922