Name: rs199738928
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.

rs199738928

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:81744304-81744319 (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)₆ / del(T)₅ / del(T)₄ / delT…
del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₁₅
Variation Type: Indel Insertion and Deletion
Frequency: (T)₁₆=0.3604 (2576/7148, ALFA)
(T)₁₆=0.4429 (2218/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: HGF : 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	7148	TTTTTTTTTTTTTTTT=0.3604	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0004, TTTTTTTTTTTTT=0.6244, TTTTTTTTTTTTTT=0.0133, TTTTTTTTTTTTTTT=0.0011, TTTTTTTTTTTTTTTTT=0.0004, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	0.150922	0.416475	0.432604	9
European	Sub	6942	TTTTTTTTTTTTTTTT=0.3544	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0004, TTTTTTTTTTTTT=0.6299, TTTTTTTTTTTTTT=0.0137, TTTTTTTTTTTTTTT=0.0012, TTTTTTTTTTTTTTTTT=0.0004, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	0.141585	0.419115	0.439299	5
African	Sub	132	TTTTTTTTTTTTTTTT=0.576	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.424, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	0.454545	0.30303	0.242424	10
African Others	Sub	6	TTTTTTTTTTTTTTTT=0.2	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.8, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	0.0	0.666667	0.333333	0
African American	Sub	126	TTTTTTTTTTTTTTTT=0.595	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.405, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	0.47619	0.285714	0.238095	9
Asian	Sub	10	TTTTTTTTTTTTTTTT=0.7	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.3, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	0.6	0.2	0.2	1
East Asian	Sub	8	TTTTTTTTTTTTTTTT=0.8	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.2, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	0.75	0.25	0.0	3
Other Asian	Sub	2	TTTTTTTTTTTTTTTT=0.5	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.5, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	0.0	0.0	1.0	1
Latin American 1	Sub	2	TTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	10	TTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	10	TTTTTTTTTTTTTTTT=0.6	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.4, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	0.6	0.4	0.0	3
Other	Sub	42	TTTTTTTTTTTTTTTT=0.36	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.64, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	0.238095	0.52381	0.238095	3

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	7148	(T)₁₆=0.3604	del(T)₅=0.0000, del(T)₄=0.0004, delTTT=0.6244, delTT=0.0133, delT=0.0011, dupT=0.0004, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	European	Sub	6942	(T)₁₆=0.3544	del(T)₅=0.0000, del(T)₄=0.0004, delTTT=0.6299, delTT=0.0137, delT=0.0012, dupT=0.0004, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	African	Sub	132	(T)₁₆=0.576	del(T)₅=0.000, del(T)₄=0.000, delTTT=0.424, 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	42	(T)₁₆=0.36	del(T)₅=0.00, del(T)₄=0.00, delTTT=0.64, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Latin American 2	Sub	10	(T)₁₆=1.0	del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0
Allele Frequency Aggregator	South Asian	Sub	10	(T)₁₆=0.6	del(T)₅=0.0, del(T)₄=0.0, delTTT=0.4, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0
Allele Frequency Aggregator	Asian	Sub	10	(T)₁₆=0.7	del(T)₅=0.0, del(T)₄=0.0, delTTT=0.3, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0
Allele Frequency Aggregator	Latin American 1	Sub	2	(T)₁₆=1.0	del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0
1000Genomes	Global	Study-wide	5008	(T)₁₆=0.4429	delTTT=0.5571
1000Genomes	African	Sub	1322	(T)₁₆=0.4879	delTTT=0.5121
1000Genomes	East Asian	Sub	1008	(T)₁₆=0.3909	delTTT=0.6091
1000Genomes	Europe	Sub	1006	(T)₁₆=0.4533	delTTT=0.5467
1000Genomes	South Asian	Sub	978	(T)₁₆=0.433	delTTT=0.567
1000Genomes	American	Sub	694	(T)₁₆=0.432	delTTT=0.568

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 7	NC_000007.14:g.81744314_81744319del
GRCh38.p14 chr 7	NC_000007.14:g.81744315_81744319del
GRCh38.p14 chr 7	NC_000007.14:g.81744316_81744319del
GRCh38.p14 chr 7	NC_000007.14:g.81744317_81744319del
GRCh38.p14 chr 7	NC_000007.14:g.81744318_81744319del
GRCh38.p14 chr 7	NC_000007.14:g.81744319del
GRCh38.p14 chr 7	NC_000007.14:g.81744319dup
GRCh38.p14 chr 7	NC_000007.14:g.81744318_81744319dup
GRCh38.p14 chr 7	NC_000007.14:g.81744317_81744319dup
GRCh38.p14 chr 7	NC_000007.14:g.81744316_81744319dup
GRCh38.p14 chr 7	NC_000007.14:g.81744315_81744319dup
GRCh38.p14 chr 7	NC_000007.14:g.81744305_81744319dup
GRCh37.p13 chr 7	NC_000007.13:g.81373630_81373635del
GRCh37.p13 chr 7	NC_000007.13:g.81373631_81373635del
GRCh37.p13 chr 7	NC_000007.13:g.81373632_81373635del
GRCh37.p13 chr 7	NC_000007.13:g.81373633_81373635del
GRCh37.p13 chr 7	NC_000007.13:g.81373634_81373635del
GRCh37.p13 chr 7	NC_000007.13:g.81373635del
GRCh37.p13 chr 7	NC_000007.13:g.81373635dup
GRCh37.p13 chr 7	NC_000007.13:g.81373634_81373635dup
GRCh37.p13 chr 7	NC_000007.13:g.81373633_81373635dup
GRCh37.p13 chr 7	NC_000007.13:g.81373632_81373635dup
GRCh37.p13 chr 7	NC_000007.13:g.81373631_81373635dup
GRCh37.p13 chr 7	NC_000007.13:g.81373621_81373635dup
HGF RefSeqGene	NG_016274.2:g.30828_30833del
HGF RefSeqGene	NG_016274.2:g.30829_30833del
HGF RefSeqGene	NG_016274.2:g.30830_30833del
HGF RefSeqGene	NG_016274.2:g.30831_30833del
HGF RefSeqGene	NG_016274.2:g.30832_30833del
HGF RefSeqGene	NG_016274.2:g.30833del
HGF RefSeqGene	NG_016274.2:g.30833dup
HGF RefSeqGene	NG_016274.2:g.30832_30833dup
HGF RefSeqGene	NG_016274.2:g.30831_30833dup
HGF RefSeqGene	NG_016274.2:g.30830_30833dup
HGF RefSeqGene	NG_016274.2:g.30829_30833dup
HGF RefSeqGene	NG_016274.2:g.30819_30833dup

Gene: HGF, hepatocyte growth factor (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
HGF transcript variant 1	NM_000601.6:c.746+691_746… NM_000601.6:c.746+691_746+696del	N/A	Intron Variant
HGF transcript variant 2	NM_001010931.3:c.746+691_… NM_001010931.3:c.746+691_746+696del	N/A	Intron Variant
HGF transcript variant 3	NM_001010932.3:c.731+691_… NM_001010932.3:c.731+691_731+696del	N/A	Intron Variant
HGF transcript variant 4	NM_001010933.3:c.731+691_… NM_001010933.3:c.731+691_731+696del	N/A	Intron Variant
HGF transcript variant 5	NM_001010934.3:c.	N/A	Genic Downstream Transcript Variant
HGF transcript variant X1	XM_047420293.1:c.746+691_… XM_047420293.1:c.746+691_746+696del	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)₁₆=	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₁₅
GRCh38.p14 chr 7	NC_000007.14:g.81744304_81744319=	NC_000007.14:g.81744314_81744319del	NC_000007.14:g.81744315_81744319del	NC_000007.14:g.81744316_81744319del	NC_000007.14:g.81744317_81744319del	NC_000007.14:g.81744318_81744319del	NC_000007.14:g.81744319del	NC_000007.14:g.81744319dup	NC_000007.14:g.81744318_81744319dup	NC_000007.14:g.81744317_81744319dup	NC_000007.14:g.81744316_81744319dup	NC_000007.14:g.81744315_81744319dup	NC_000007.14:g.81744305_81744319dup
GRCh37.p13 chr 7	NC_000007.13:g.81373620_81373635=	NC_000007.13:g.81373630_81373635del	NC_000007.13:g.81373631_81373635del	NC_000007.13:g.81373632_81373635del	NC_000007.13:g.81373633_81373635del	NC_000007.13:g.81373634_81373635del	NC_000007.13:g.81373635del	NC_000007.13:g.81373635dup	NC_000007.13:g.81373634_81373635dup	NC_000007.13:g.81373633_81373635dup	NC_000007.13:g.81373632_81373635dup	NC_000007.13:g.81373631_81373635dup	NC_000007.13:g.81373621_81373635dup
HGF RefSeqGene	NG_016274.2:g.30818_30833=	NG_016274.2:g.30828_30833del	NG_016274.2:g.30829_30833del	NG_016274.2:g.30830_30833del	NG_016274.2:g.30831_30833del	NG_016274.2:g.30832_30833del	NG_016274.2:g.30833del	NG_016274.2:g.30833dup	NG_016274.2:g.30832_30833dup	NG_016274.2:g.30831_30833dup	NG_016274.2:g.30830_30833dup	NG_016274.2:g.30829_30833dup	NG_016274.2:g.30819_30833dup
HGF transcript variant 1	NM_000601.4:c.746+696=	NM_000601.4:c.746+691_746+696del	NM_000601.4:c.746+692_746+696del	NM_000601.4:c.746+693_746+696del	NM_000601.4:c.746+694_746+696del	NM_000601.4:c.746+695_746+696del	NM_000601.4:c.746+696del	NM_000601.4:c.746+696dup	NM_000601.4:c.746+695_746+696dup	NM_000601.4:c.746+694_746+696dup	NM_000601.4:c.746+693_746+696dup	NM_000601.4:c.746+692_746+696dup	NM_000601.4:c.746+682_746+696dup
HGF transcript variant 1	NM_000601.6:c.746+696=	NM_000601.6:c.746+691_746+696del	NM_000601.6:c.746+692_746+696del	NM_000601.6:c.746+693_746+696del	NM_000601.6:c.746+694_746+696del	NM_000601.6:c.746+695_746+696del	NM_000601.6:c.746+696del	NM_000601.6:c.746+696dup	NM_000601.6:c.746+695_746+696dup	NM_000601.6:c.746+694_746+696dup	NM_000601.6:c.746+693_746+696dup	NM_000601.6:c.746+692_746+696dup	NM_000601.6:c.746+682_746+696dup
HGF transcript variant 2	NM_001010931.1:c.746+696=	NM_001010931.1:c.746+691_746+696del	NM_001010931.1:c.746+692_746+696del	NM_001010931.1:c.746+693_746+696del	NM_001010931.1:c.746+694_746+696del	NM_001010931.1:c.746+695_746+696del	NM_001010931.1:c.746+696del	NM_001010931.1:c.746+696dup	NM_001010931.1:c.746+695_746+696dup	NM_001010931.1:c.746+694_746+696dup	NM_001010931.1:c.746+693_746+696dup	NM_001010931.1:c.746+692_746+696dup	NM_001010931.1:c.746+682_746+696dup
HGF transcript variant 2	NM_001010931.3:c.746+696=	NM_001010931.3:c.746+691_746+696del	NM_001010931.3:c.746+692_746+696del	NM_001010931.3:c.746+693_746+696del	NM_001010931.3:c.746+694_746+696del	NM_001010931.3:c.746+695_746+696del	NM_001010931.3:c.746+696del	NM_001010931.3:c.746+696dup	NM_001010931.3:c.746+695_746+696dup	NM_001010931.3:c.746+694_746+696dup	NM_001010931.3:c.746+693_746+696dup	NM_001010931.3:c.746+692_746+696dup	NM_001010931.3:c.746+682_746+696dup
HGF transcript variant 3	NM_001010932.1:c.731+696=	NM_001010932.1:c.731+691_731+696del	NM_001010932.1:c.731+692_731+696del	NM_001010932.1:c.731+693_731+696del	NM_001010932.1:c.731+694_731+696del	NM_001010932.1:c.731+695_731+696del	NM_001010932.1:c.731+696del	NM_001010932.1:c.731+696dup	NM_001010932.1:c.731+695_731+696dup	NM_001010932.1:c.731+694_731+696dup	NM_001010932.1:c.731+693_731+696dup	NM_001010932.1:c.731+692_731+696dup	NM_001010932.1:c.731+682_731+696dup
HGF transcript variant 3	NM_001010932.3:c.731+696=	NM_001010932.3:c.731+691_731+696del	NM_001010932.3:c.731+692_731+696del	NM_001010932.3:c.731+693_731+696del	NM_001010932.3:c.731+694_731+696del	NM_001010932.3:c.731+695_731+696del	NM_001010932.3:c.731+696del	NM_001010932.3:c.731+696dup	NM_001010932.3:c.731+695_731+696dup	NM_001010932.3:c.731+694_731+696dup	NM_001010932.3:c.731+693_731+696dup	NM_001010932.3:c.731+692_731+696dup	NM_001010932.3:c.731+682_731+696dup
HGF transcript variant 4	NM_001010933.1:c.731+696=	NM_001010933.1:c.731+691_731+696del	NM_001010933.1:c.731+692_731+696del	NM_001010933.1:c.731+693_731+696del	NM_001010933.1:c.731+694_731+696del	NM_001010933.1:c.731+695_731+696del	NM_001010933.1:c.731+696del	NM_001010933.1:c.731+696dup	NM_001010933.1:c.731+695_731+696dup	NM_001010933.1:c.731+694_731+696dup	NM_001010933.1:c.731+693_731+696dup	NM_001010933.1:c.731+692_731+696dup	NM_001010933.1:c.731+682_731+696dup
HGF transcript variant 4	NM_001010933.3:c.731+696=	NM_001010933.3:c.731+691_731+696del	NM_001010933.3:c.731+692_731+696del	NM_001010933.3:c.731+693_731+696del	NM_001010933.3:c.731+694_731+696del	NM_001010933.3:c.731+695_731+696del	NM_001010933.3:c.731+696del	NM_001010933.3:c.731+696dup	NM_001010933.3:c.731+695_731+696dup	NM_001010933.3:c.731+694_731+696dup	NM_001010933.3:c.731+693_731+696dup	NM_001010933.3:c.731+692_731+696dup	NM_001010933.3:c.731+682_731+696dup
HGF transcript variant X1	XM_047420293.1:c.746+696=	XM_047420293.1:c.746+691_746+696del	XM_047420293.1:c.746+692_746+696del	XM_047420293.1:c.746+693_746+696del	XM_047420293.1:c.746+694_746+696del	XM_047420293.1:c.746+695_746+696del	XM_047420293.1:c.746+696del	XM_047420293.1:c.746+696dup	XM_047420293.1:c.746+695_746+696dup	XM_047420293.1:c.746+694_746+696dup	XM_047420293.1:c.746+693_746+696dup	XM_047420293.1:c.746+692_746+696dup	XM_047420293.1:c.746+682_746+696dup

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#.

68 SubSNP, 31 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80202854	Aug 21, 2014 (142)
2	HGSV	ss80506578	Aug 21, 2014 (142)
3	HGSV	ss82008266	Aug 21, 2014 (142)
4	GMI	ss288853586	May 04, 2012 (137)
5	PJP	ss295343693	Aug 21, 2014 (142)
6	BILGI_BIOE	ss666405549	Apr 25, 2013 (138)
7	SSIP	ss947199779	Aug 21, 2014 (142)
8	1000GENOMES	ss1377293804	Aug 21, 2014 (142)
9	DDI	ss1536553021	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1705702165	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1705702194	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1710333153	Apr 01, 2015 (144)
13	EVA_UK10K_TWINSUK	ss1710338425	Apr 01, 2015 (144)
14	HAMMER_LAB	ss1805081337	Sep 08, 2015 (146)
15	SWEGEN	ss3001512487	Nov 08, 2017 (151)
16	MCHAISSO	ss3064262061	Nov 08, 2017 (151)
17	MCHAISSO	ss3065144773	Nov 08, 2017 (151)
18	MCHAISSO	ss3066153853	Nov 08, 2017 (151)
19	BIOINF_KMB_FNS_UNIBA	ss3646039658	Oct 12, 2018 (152)
20	URBANLAB	ss3648684698	Oct 12, 2018 (152)
21	EVA_DECODE	ss3720069631	Jul 13, 2019 (153)
22	EVA_DECODE	ss3720069632	Jul 13, 2019 (153)
23	EVA_DECODE	ss3720069633	Jul 13, 2019 (153)
24	EVA_DECODE	ss3720069634	Jul 13, 2019 (153)
25	EVA_DECODE	ss3720069635	Jul 13, 2019 (153)
26	EVA_DECODE	ss3720069636	Jul 13, 2019 (153)
27	ACPOP	ss3734799049	Jul 13, 2019 (153)
28	ACPOP	ss3734799050	Jul 13, 2019 (153)
29	PACBIO	ss3785873315	Jul 13, 2019 (153)
30	PACBIO	ss3791167105	Jul 13, 2019 (153)
31	PACBIO	ss3796047016	Jul 13, 2019 (153)
32	KHV_HUMAN_GENOMES	ss3809951339	Jul 13, 2019 (153)
33	EVA	ss3830665737	Apr 26, 2020 (154)
34	EVA	ss3838829639	Apr 26, 2020 (154)
35	EVA	ss3844284141	Apr 26, 2020 (154)
36	KOGIC	ss3961955923	Apr 26, 2020 (154)
37	KOGIC	ss3961955924	Apr 26, 2020 (154)
38	KOGIC	ss3961955925	Apr 26, 2020 (154)
39	KOGIC	ss3961955926	Apr 26, 2020 (154)
40	KOGIC	ss3961955927	Apr 26, 2020 (154)
41	GNOMAD	ss4167187449	Apr 26, 2021 (155)
42	GNOMAD	ss4167187450	Apr 26, 2021 (155)
43	GNOMAD	ss4167187452	Apr 26, 2021 (155)
44	GNOMAD	ss4167187453	Apr 26, 2021 (155)
45	GNOMAD	ss4167187454	Apr 26, 2021 (155)
46	GNOMAD	ss4167187455	Apr 26, 2021 (155)
47	GNOMAD	ss4167187456	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5184106872	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5184106873	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5184106874	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5184106875	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5184106876	Apr 26, 2021 (155)
53	1000G_HIGH_COVERAGE	ss5273607595	Oct 13, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5273607596	Oct 13, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5273607597	Oct 13, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5273607598	Oct 13, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5273607599	Oct 13, 2022 (156)
58	HUGCELL_USP	ss5470619857	Oct 13, 2022 (156)
59	HUGCELL_USP	ss5470619858	Oct 13, 2022 (156)
60	HUGCELL_USP	ss5470619859	Oct 13, 2022 (156)
61	TOMMO_GENOMICS	ss5724654065	Oct 13, 2022 (156)
62	TOMMO_GENOMICS	ss5724654066	Oct 13, 2022 (156)
63	TOMMO_GENOMICS	ss5724654067	Oct 13, 2022 (156)
64	TOMMO_GENOMICS	ss5724654068	Oct 13, 2022 (156)
65	TOMMO_GENOMICS	ss5724654069	Oct 13, 2022 (156)
66	EVA	ss5823094318	Oct 13, 2022 (156)
67	EVA	ss5823094319	Oct 13, 2022 (156)
68	EVA	ss5859604890	Oct 13, 2022 (156)
69	1000Genomes	NC_000007.13 - 81373620	Oct 12, 2018 (152)
70	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 21064451 (NC_000007.13:81373620:TT: 3215/3854) Row 21064452 (NC_000007.13:81373619:TTTT: 297/3854)	-	Oct 12, 2018 (152)
71	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 21064451 (NC_000007.13:81373620:TT: 3215/3854) Row 21064452 (NC_000007.13:81373619:TTTT: 297/3854)	-	Oct 12, 2018 (152)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 267016061 (NC_000007.14:81744303::T 49/134826) Row 267016062 (NC_000007.14:81744303::TTTT 1/134828) Row 267016064 (NC_000007.14:81744303:T: 3553/134752)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 267016061 (NC_000007.14:81744303::T 49/134826) Row 267016062 (NC_000007.14:81744303::TTTT 1/134828) Row 267016064 (NC_000007.14:81744303:T: 3553/134752)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 267016061 (NC_000007.14:81744303::T 49/134826) Row 267016062 (NC_000007.14:81744303::TTTT 1/134828) Row 267016064 (NC_000007.14:81744303:T: 3553/134752)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 267016061 (NC_000007.14:81744303::T 49/134826) Row 267016062 (NC_000007.14:81744303::TTTT 1/134828) Row 267016064 (NC_000007.14:81744303:T: 3553/134752)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 267016061 (NC_000007.14:81744303::T 49/134826) Row 267016062 (NC_000007.14:81744303::TTTT 1/134828) Row 267016064 (NC_000007.14:81744303:T: 3553/134752)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 267016061 (NC_000007.14:81744303::T 49/134826) Row 267016062 (NC_000007.14:81744303::TTTT 1/134828) Row 267016064 (NC_000007.14:81744303:T: 3553/134752)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 267016061 (NC_000007.14:81744303::T 49/134826) Row 267016062 (NC_000007.14:81744303::TTTT 1/134828) Row 267016064 (NC_000007.14:81744303:T: 3553/134752)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 267016061 (NC_000007.14:81744303::T 49/134826) Row 267016062 (NC_000007.14:81744303::TTTT 1/134828) Row 267016064 (NC_000007.14:81744303:T: 3553/134752)...	-	Apr 26, 2021 (155)
80	Korean Genome Project Submission ignored due to conflicting rows: Row 18333924 (NC_000007.14:81744304:TTT: 1446/1832) Row 18333925 (NC_000007.14:81744305:TT: 35/1832) Row 18333926 (NC_000007.14:81744303:TTTT: 54/1832)...	-	Apr 26, 2020 (154)
81	Korean Genome Project Submission ignored due to conflicting rows: Row 18333924 (NC_000007.14:81744304:TTT: 1446/1832) Row 18333925 (NC_000007.14:81744305:TT: 35/1832) Row 18333926 (NC_000007.14:81744303:TTTT: 54/1832)...	-	Apr 26, 2020 (154)
82	Korean Genome Project Submission ignored due to conflicting rows: Row 18333924 (NC_000007.14:81744304:TTT: 1446/1832) Row 18333925 (NC_000007.14:81744305:TT: 35/1832) Row 18333926 (NC_000007.14:81744303:TTTT: 54/1832)...	-	Apr 26, 2020 (154)
83	Korean Genome Project Submission ignored due to conflicting rows: Row 18333924 (NC_000007.14:81744304:TTT: 1446/1832) Row 18333925 (NC_000007.14:81744305:TT: 35/1832) Row 18333926 (NC_000007.14:81744303:TTTT: 54/1832)...	-	Apr 26, 2020 (154)
84	Korean Genome Project Submission ignored due to conflicting rows: Row 18333924 (NC_000007.14:81744304:TTT: 1446/1832) Row 18333925 (NC_000007.14:81744305:TT: 35/1832) Row 18333926 (NC_000007.14:81744303:TTTT: 54/1832)...	-	Apr 26, 2020 (154)
85	Northern Sweden Submission ignored due to conflicting rows: Row 8083914 (NC_000007.13:81373619:TTT: 424/600) Row 8083915 (NC_000007.13:81373619:TT: 8/600)	-	Jul 13, 2019 (153)
86	Northern Sweden Submission ignored due to conflicting rows: Row 8083914 (NC_000007.13:81373619:TTT: 424/600) Row 8083915 (NC_000007.13:81373619:TT: 8/600)	-	Jul 13, 2019 (153)
87	8.3KJPN Submission ignored due to conflicting rows: Row 42076179 (NC_000007.13:81373619:TTTT: 57/16758) Row 42076180 (NC_000007.13:81373619:TTT: 14512/16758) Row 42076181 (NC_000007.13:81373619:T: 11/16758)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 42076179 (NC_000007.13:81373619:TTTT: 57/16758) Row 42076180 (NC_000007.13:81373619:TTT: 14512/16758) Row 42076181 (NC_000007.13:81373619:T: 11/16758)...	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 42076179 (NC_000007.13:81373619:TTTT: 57/16758) Row 42076180 (NC_000007.13:81373619:TTT: 14512/16758) Row 42076181 (NC_000007.13:81373619:T: 11/16758)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 42076179 (NC_000007.13:81373619:TTTT: 57/16758) Row 42076180 (NC_000007.13:81373619:TTT: 14512/16758) Row 42076181 (NC_000007.13:81373619:T: 11/16758)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 42076179 (NC_000007.13:81373619:TTTT: 57/16758) Row 42076180 (NC_000007.13:81373619:TTT: 14512/16758) Row 42076181 (NC_000007.13:81373619:T: 11/16758)...	-	Apr 26, 2021 (155)
92	14KJPN Submission ignored due to conflicting rows: Row 58491169 (NC_000007.14:81744303:TTT: 24448/28258) Row 58491170 (NC_000007.14:81744303:TTTT: 83/28258) Row 58491171 (NC_000007.14:81744303:T: 15/28258)...	-	Oct 13, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 58491169 (NC_000007.14:81744303:TTT: 24448/28258) Row 58491170 (NC_000007.14:81744303:TTTT: 83/28258) Row 58491171 (NC_000007.14:81744303:T: 15/28258)...	-	Oct 13, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 58491169 (NC_000007.14:81744303:TTT: 24448/28258) Row 58491170 (NC_000007.14:81744303:TTTT: 83/28258) Row 58491171 (NC_000007.14:81744303:T: 15/28258)...	-	Oct 13, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 58491169 (NC_000007.14:81744303:TTT: 24448/28258) Row 58491170 (NC_000007.14:81744303:TTTT: 83/28258) Row 58491171 (NC_000007.14:81744303:T: 15/28258)...	-	Oct 13, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 58491169 (NC_000007.14:81744303:TTT: 24448/28258) Row 58491170 (NC_000007.14:81744303:TTTT: 83/28258) Row 58491171 (NC_000007.14:81744303:T: 15/28258)...	-	Oct 13, 2022 (156)
97	UK 10K study - Twins Submission ignored due to conflicting rows: Row 21064451 (NC_000007.13:81373620:TT: 3023/3708) Row 21064452 (NC_000007.13:81373619:TTTT: 293/3708)	-	Oct 12, 2018 (152)
98	UK 10K study - Twins Submission ignored due to conflicting rows: Row 21064451 (NC_000007.13:81373620:TT: 3023/3708) Row 21064452 (NC_000007.13:81373619:TTTT: 293/3708)	-	Oct 12, 2018 (152)
99	ALFA	NC_000007.14 - 81744304	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)
rs57601785	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4167187456	NC_000007.14:81744303:TTTTTT:	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4167187455	NC_000007.14:81744303:TTTTT:	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
5675587900	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss1705702165, ss1705702194, ss5184106872, ss5823094319	NC_000007.13:81373619:TTTT:	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3720069631, ss3961955925, ss4167187454, ss5273607597, ss5724654066	NC_000007.14:81744303:TTTT:	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
5675587900	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss80202854, ss80506578, ss82008266	NC_000007.11:81018283:TTT:	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss288853586, ss295343693	NC_000007.12:81211555:TTT:	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
37851048, ss666405549, ss1377293804, ss1536553021, ss1805081337, ss3001512487, ss3734799049, ss3785873315, ss3791167105, ss3796047016, ss3830665737, ss3838829639, ss5184106873, ss5823094318	NC_000007.13:81373619:TTT:	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss947199779, ss1710333153, ss1710338425	NC_000007.13:81373620:TTT:	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3064262061, ss3065144773, ss3066153853, ss3646039658, ss3648684698, ss3809951339, ss3844284141, ss4167187453, ss5273607595, ss5470619858, ss5724654065, ss5859604890	NC_000007.14:81744303:TTT:	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
5675587900	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3720069632, ss3961955923	NC_000007.14:81744304:TTT:	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3734799050, ss5184106875	NC_000007.13:81373619:TT:	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
	NC_000007.13:81373620:TT:	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4167187452, ss5273607596, ss5470619857, ss5724654068	NC_000007.14:81744303:TT:	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
5675587900	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3720069633, ss3961955924	NC_000007.14:81744305:TT:	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss5184106874	NC_000007.13:81373619:T:	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5273607598, ss5470619859, ss5724654067	NC_000007.14:81744303:T:	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
5675587900	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3961955927	NC_000007.14:81744306:T:	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5184106876	NC_000007.13:81373619::T	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4167187449, ss5273607599, ss5724654069	NC_000007.14:81744303::T	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
5675587900	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3720069634, ss3961955926	NC_000007.14:81744307::T	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
5675587900	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
5675587900	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4167187450	NC_000007.14:81744303::TTTT	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
5675587900	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3720069635	NC_000007.14:81744307::TTTTT	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3720069636	NC_000007.14:81744307::TTTTTTTTTTT… NC_000007.14:81744307::TTTTTTTTTTTTTTT	NC_000007.14:81744303:TTTTTTTTTTTT… NC_000007.14:81744303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs199738928

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

rs199738928