Name: rs34150957
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.

rs34150957

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:130471075-130471101 (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(GT)₆ / del(GT)₅ / del(GT)₄ / d…
del(GT)₆ / del(GT)₅ / del(GT)₄ / del(GT)₃ / delGTGT / delGT / dupGT / dupGTGT / dup(GT)₃ / dup(GT)₄ / dup(GT)₅
Variation Type: Indel Insertion and Deletion
Frequency: (TG)₁₃T=0.3642 (2153/5911, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: COL6A5 : 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	5911	TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.3642	TGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0088, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.5931, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0335, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0003, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.28714	0.507761	0.2051	32
European	Sub	4921	TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.2380	TGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0106, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.7108, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0402, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0004, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.129353	0.619629	0.251018	32
African	Sub	774	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	TGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	38	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
African American	Sub	736	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	TGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	22	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	18	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0	TGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	16	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	94	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	10	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0	TGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Other	Sub	74	TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.89	TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.11, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	0.891892	0.108108	0.0	20

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	5911	(TG)₁₃T=0.3642	del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0088, delGT=0.0000, dupGT=0.5931, dupGTGT=0.0335, dup(GT)₃=0.0003, dup(GT)₄=0.0000, dup(GT)₅=0.0000
Allele Frequency Aggregator	European	Sub	4921	(TG)₁₃T=0.2380	del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0106, delGT=0.0000, dupGT=0.7108, dupGTGT=0.0402, dup(GT)₃=0.0004, dup(GT)₄=0.0000, dup(GT)₅=0.0000
Allele Frequency Aggregator	African	Sub	774	(TG)₁₃T=1.000	del(GT)₆=0.000, del(GT)₅=0.000, del(GT)₄=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	94	(TG)₁₃T=1.00	del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00
Allele Frequency Aggregator	Other	Sub	74	(TG)₁₃T=0.89	del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.11, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00
Allele Frequency Aggregator	Asian	Sub	22	(TG)₁₃T=1.00	del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	16	(TG)₁₃T=1.00	del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	10	(TG)₁₃T=1.0	del(GT)₆=0.0, del(GT)₅=0.0, del(GT)₄=0.0, del(GT)₃=0.0, delGTGT=0.0, delGT=0.0, dupGT=0.0, dupGTGT=0.0, dup(GT)₃=0.0, dup(GT)₄=0.0, dup(GT)₅=0.0

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 3	NC_000003.12:g.130471076GT[7]
GRCh38.p14 chr 3	NC_000003.12:g.130471076GT[8]
GRCh38.p14 chr 3	NC_000003.12:g.130471076GT[9]
GRCh38.p14 chr 3	NC_000003.12:g.130471076GT[10]
GRCh38.p14 chr 3	NC_000003.12:g.130471076GT[11]
GRCh38.p14 chr 3	NC_000003.12:g.130471076GT[12]
GRCh38.p14 chr 3	NC_000003.12:g.130471076GT[14]
GRCh38.p14 chr 3	NC_000003.12:g.130471076GT[15]
GRCh38.p14 chr 3	NC_000003.12:g.130471076GT[16]
GRCh38.p14 chr 3	NC_000003.12:g.130471076GT[17]
GRCh38.p14 chr 3	NC_000003.12:g.130471076GT[18]
GRCh37.p13 chr 3	NC_000003.11:g.130189920GT[7]
GRCh37.p13 chr 3	NC_000003.11:g.130189920GT[8]
GRCh37.p13 chr 3	NC_000003.11:g.130189920GT[9]
GRCh37.p13 chr 3	NC_000003.11:g.130189920GT[10]
GRCh37.p13 chr 3	NC_000003.11:g.130189920GT[11]
GRCh37.p13 chr 3	NC_000003.11:g.130189920GT[12]
GRCh37.p13 chr 3	NC_000003.11:g.130189920GT[14]
GRCh37.p13 chr 3	NC_000003.11:g.130189920GT[15]
GRCh37.p13 chr 3	NC_000003.11:g.130189920GT[16]
GRCh37.p13 chr 3	NC_000003.11:g.130189920GT[17]
GRCh37.p13 chr 3	NC_000003.11:g.130189920GT[18]
COL6A5 RefSeqGene	NG_021424.1:g.130562GT[7]
COL6A5 RefSeqGene	NG_021424.1:g.130562GT[8]
COL6A5 RefSeqGene	NG_021424.1:g.130562GT[9]
COL6A5 RefSeqGene	NG_021424.1:g.130562GT[10]
COL6A5 RefSeqGene	NG_021424.1:g.130562GT[11]
COL6A5 RefSeqGene	NG_021424.1:g.130562GT[12]
COL6A5 RefSeqGene	NG_021424.1:g.130562GT[14]
COL6A5 RefSeqGene	NG_021424.1:g.130562GT[15]
COL6A5 RefSeqGene	NG_021424.1:g.130562GT[16]
COL6A5 RefSeqGene	NG_021424.1:g.130562GT[17]
COL6A5 RefSeqGene	NG_021424.1:g.130562GT[18]

Gene: COL6A5, collagen type VI alpha 5 chain (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
COL6A5 transcript variant 1	NM_001278298.2:c.7574+108… NM_001278298.2:c.7574+108TG[7]	N/A	Intron Variant
COL6A5 transcript variant 2	NM_153264.7:c.7574+108TG[… NM_153264.7:c.7574+108TG[7]	N/A	Intron Variant
COL6A5 transcript variant 3	NR_022012.3:n.	N/A	Intron Variant
COL6A5 transcript variant X1	XM_011512622.3:c.	N/A	Genic Downstream Transcript Variant
COL6A5 transcript variant X2	XM_011512623.3:c.	N/A	Genic Downstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(TG)₁₃T=	del(GT)₆	del(GT)₅	del(GT)₄	del(GT)₃	delGTGT	delGT	dupGT	dupGTGT	dup(GT)₃	dup(GT)₄	dup(GT)₅
GRCh38.p14 chr 3	NC_000003.12:g.130471075_130471101=	NC_000003.12:g.130471076GT[7]	NC_000003.12:g.130471076GT[8]	NC_000003.12:g.130471076GT[9]	NC_000003.12:g.130471076GT[10]	NC_000003.12:g.130471076GT[11]	NC_000003.12:g.130471076GT[12]	NC_000003.12:g.130471076GT[14]	NC_000003.12:g.130471076GT[15]	NC_000003.12:g.130471076GT[16]	NC_000003.12:g.130471076GT[17]	NC_000003.12:g.130471076GT[18]
GRCh37.p13 chr 3	NC_000003.11:g.130189919_130189945=	NC_000003.11:g.130189920GT[7]	NC_000003.11:g.130189920GT[8]	NC_000003.11:g.130189920GT[9]	NC_000003.11:g.130189920GT[10]	NC_000003.11:g.130189920GT[11]	NC_000003.11:g.130189920GT[12]	NC_000003.11:g.130189920GT[14]	NC_000003.11:g.130189920GT[15]	NC_000003.11:g.130189920GT[16]	NC_000003.11:g.130189920GT[17]	NC_000003.11:g.130189920GT[18]
COL6A5 RefSeqGene	NG_021424.1:g.130561_130587=	NG_021424.1:g.130562GT[7]	NG_021424.1:g.130562GT[8]	NG_021424.1:g.130562GT[9]	NG_021424.1:g.130562GT[10]	NG_021424.1:g.130562GT[11]	NG_021424.1:g.130562GT[12]	NG_021424.1:g.130562GT[14]	NG_021424.1:g.130562GT[15]	NG_021424.1:g.130562GT[16]	NG_021424.1:g.130562GT[17]	NG_021424.1:g.130562GT[18]
COL6A5 transcript variant 1	NM_001278298.1:c.7574+108=	NM_001278298.1:c.7574+108TG[7]	NM_001278298.1:c.7574+108TG[8]	NM_001278298.1:c.7574+108TG[9]	NM_001278298.1:c.7574+108TG[10]	NM_001278298.1:c.7574+108TG[11]	NM_001278298.1:c.7574+108TG[12]	NM_001278298.1:c.7574+108TG[14]	NM_001278298.1:c.7574+108TG[15]	NM_001278298.1:c.7574+108TG[16]	NM_001278298.1:c.7574+108TG[17]	NM_001278298.1:c.7574+108TG[18]
COL6A5 transcript variant 1	NM_001278298.2:c.7574+108=	NM_001278298.2:c.7574+108TG[7]	NM_001278298.2:c.7574+108TG[8]	NM_001278298.2:c.7574+108TG[9]	NM_001278298.2:c.7574+108TG[10]	NM_001278298.2:c.7574+108TG[11]	NM_001278298.2:c.7574+108TG[12]	NM_001278298.2:c.7574+108TG[14]	NM_001278298.2:c.7574+108TG[15]	NM_001278298.2:c.7574+108TG[16]	NM_001278298.2:c.7574+108TG[17]	NM_001278298.2:c.7574+108TG[18]
COL6A5 transcript variant 2	NM_153264.6:c.7574+108=	NM_153264.6:c.7574+108TG[7]	NM_153264.6:c.7574+108TG[8]	NM_153264.6:c.7574+108TG[9]	NM_153264.6:c.7574+108TG[10]	NM_153264.6:c.7574+108TG[11]	NM_153264.6:c.7574+108TG[12]	NM_153264.6:c.7574+108TG[14]	NM_153264.6:c.7574+108TG[15]	NM_153264.6:c.7574+108TG[16]	NM_153264.6:c.7574+108TG[17]	NM_153264.6:c.7574+108TG[18]
COL6A5 transcript variant 2	NM_153264.7:c.7574+108=	NM_153264.7:c.7574+108TG[7]	NM_153264.7:c.7574+108TG[8]	NM_153264.7:c.7574+108TG[9]	NM_153264.7:c.7574+108TG[10]	NM_153264.7:c.7574+108TG[11]	NM_153264.7:c.7574+108TG[12]	NM_153264.7:c.7574+108TG[14]	NM_153264.7:c.7574+108TG[15]	NM_153264.7:c.7574+108TG[16]	NM_153264.7:c.7574+108TG[17]	NM_153264.7:c.7574+108TG[18]

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#.

73 SubSNP, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41971318	Mar 15, 2006 (126)
2	HUMANGENOME_JCVI	ss95331680	Feb 13, 2009 (138)
3	GMI	ss288416735	May 04, 2012 (137)
4	GMI	ss288416737	May 04, 2012 (138)
5	1000GENOMES	ss326425009	May 09, 2011 (134)
6	1000GENOMES	ss326448416	May 09, 2011 (134)
7	LUNTER	ss551279296	Apr 25, 2013 (138)
8	LUNTER	ss551376538	Jan 10, 2018 (151)
9	LUNTER	ss553058828	Apr 25, 2013 (138)
10	SSMP	ss663355315	Apr 01, 2015 (144)
11	BILGI_BIOE	ss666226385	Apr 25, 2013 (138)
12	DDI	ss1536372586	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1703822829	Apr 01, 2015 (144)
14	EVA_UK10K_ALSPAC	ss1703822830	Apr 01, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1703823036	Apr 01, 2015 (144)
16	EVA_UK10K_TWINSUK	ss1703823037	Apr 01, 2015 (144)
17	TMC_SNPDB	ss1997161961	Oct 12, 2018 (152)
18	TMC_SNPDB	ss1997161963	Jan 10, 2018 (151)
19	SWEGEN	ss2993192447	Nov 08, 2017 (151)
20	MCHAISSO	ss3064930459	Nov 08, 2017 (151)
21	URBANLAB	ss3647526237	Oct 12, 2018 (152)
22	EVA_DECODE	ss3710282581	Jul 13, 2019 (153)
23	EVA_DECODE	ss3710282582	Jul 13, 2019 (153)
24	EVA_DECODE	ss3710282583	Jul 13, 2019 (153)
25	EVA_DECODE	ss3710282584	Jul 13, 2019 (153)
26	EVA_DECODE	ss3710282585	Jul 13, 2019 (153)
27	ACPOP	ss3730348462	Jul 13, 2019 (153)
28	ACPOP	ss3730348463	Jul 13, 2019 (153)
29	ACPOP	ss3730348464	Jul 13, 2019 (153)
30	PACBIO	ss3784463611	Jul 13, 2019 (153)
31	PACBIO	ss3789957704	Jul 13, 2019 (153)
32	PACBIO	ss3794832272	Jul 13, 2019 (153)
33	FSA-LAB	ss3984262942	Apr 26, 2021 (155)
34	FSA-LAB	ss3984262943	Apr 26, 2021 (155)
35	FSA-LAB	ss3984262944	Apr 26, 2021 (155)
36	EVA	ss3984446973	Apr 26, 2021 (155)
37	GNOMAD	ss4080731373	Apr 26, 2021 (155)
38	GNOMAD	ss4080731374	Apr 26, 2021 (155)
39	GNOMAD	ss4080731375	Apr 26, 2021 (155)
40	GNOMAD	ss4080731376	Apr 26, 2021 (155)
41	GNOMAD	ss4080731378	Apr 26, 2021 (155)
42	GNOMAD	ss4080731379	Apr 26, 2021 (155)
43	GNOMAD	ss4080731380	Apr 26, 2021 (155)
44	GNOMAD	ss4080731381	Apr 26, 2021 (155)
45	GNOMAD	ss4080731382	Apr 26, 2021 (155)
46	GNOMAD	ss4080731383	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5161570690	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5161570691	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5161570692	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5161570693	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5161570694	Apr 26, 2021 (155)
52	EVA	ss5237178775	Apr 26, 2021 (155)
53	EVA	ss5237178776	Apr 26, 2021 (155)
54	1000G_HIGH_COVERAGE	ss5256015629	Oct 12, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5256015630	Oct 12, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5256015631	Oct 12, 2022 (156)
57	HUGCELL_USP	ss5455157373	Oct 12, 2022 (156)
58	HUGCELL_USP	ss5455157374	Oct 12, 2022 (156)
59	HUGCELL_USP	ss5455157375	Oct 12, 2022 (156)
60	HUGCELL_USP	ss5455157376	Oct 12, 2022 (156)
61	HUGCELL_USP	ss5455157377	Oct 12, 2022 (156)
62	EVA	ss5624132314	Oct 12, 2022 (156)
63	EVA	ss5624132315	Oct 12, 2022 (156)
64	TOMMO_GENOMICS	ss5694445077	Oct 12, 2022 (156)
65	TOMMO_GENOMICS	ss5694445078	Oct 12, 2022 (156)
66	TOMMO_GENOMICS	ss5694445079	Oct 12, 2022 (156)
67	TOMMO_GENOMICS	ss5694445080	Oct 12, 2022 (156)
68	TOMMO_GENOMICS	ss5694445081	Oct 12, 2022 (156)
69	EVA	ss5800109831	Oct 12, 2022 (156)
70	EVA	ss5826477639	Oct 12, 2022 (156)
71	EVA	ss5826477640	Oct 12, 2022 (156)
72	EVA	ss5848592960	Oct 12, 2022 (156)
73	EVA	ss5980173762	Oct 12, 2022 (156)
74	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 9693216 (NC_000003.11:130189918::TG 2728/3854) Row 9693217 (NC_000003.11:130189918::TGTG 162/3854)	-	Oct 12, 2018 (152)
75	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 9693216 (NC_000003.11:130189918::TG 2728/3854) Row 9693217 (NC_000003.11:130189918::TGTG 162/3854)	-	Oct 12, 2018 (152)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 123691092 (NC_000003.12:130471074::TG 77725/132618) Row 123691093 (NC_000003.12:130471074::TGTG 4779/132672) Row 123691094 (NC_000003.12:130471074::TGTGTG 516/132718)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 123691092 (NC_000003.12:130471074::TG 77725/132618) Row 123691093 (NC_000003.12:130471074::TGTG 4779/132672) Row 123691094 (NC_000003.12:130471074::TGTGTG 516/132718)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 123691092 (NC_000003.12:130471074::TG 77725/132618) Row 123691093 (NC_000003.12:130471074::TGTG 4779/132672) Row 123691094 (NC_000003.12:130471074::TGTGTG 516/132718)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 123691092 (NC_000003.12:130471074::TG 77725/132618) Row 123691093 (NC_000003.12:130471074::TGTG 4779/132672) Row 123691094 (NC_000003.12:130471074::TGTGTG 516/132718)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 123691092 (NC_000003.12:130471074::TG 77725/132618) Row 123691093 (NC_000003.12:130471074::TGTG 4779/132672) Row 123691094 (NC_000003.12:130471074::TGTGTG 516/132718)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 123691092 (NC_000003.12:130471074::TG 77725/132618) Row 123691093 (NC_000003.12:130471074::TGTG 4779/132672) Row 123691094 (NC_000003.12:130471074::TGTGTG 516/132718)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 123691092 (NC_000003.12:130471074::TG 77725/132618) Row 123691093 (NC_000003.12:130471074::TGTG 4779/132672) Row 123691094 (NC_000003.12:130471074::TGTGTG 516/132718)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 123691092 (NC_000003.12:130471074::TG 77725/132618) Row 123691093 (NC_000003.12:130471074::TGTG 4779/132672) Row 123691094 (NC_000003.12:130471074::TGTGTG 516/132718)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 123691092 (NC_000003.12:130471074::TG 77725/132618) Row 123691093 (NC_000003.12:130471074::TGTG 4779/132672) Row 123691094 (NC_000003.12:130471074::TGTGTG 516/132718)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 123691092 (NC_000003.12:130471074::TG 77725/132618) Row 123691093 (NC_000003.12:130471074::TGTG 4779/132672) Row 123691094 (NC_000003.12:130471074::TGTGTG 516/132718)...	-	Apr 26, 2021 (155)
86	Northern Sweden Submission ignored due to conflicting rows: Row 3633327 (NC_000003.11:130189918::TG 453/600) Row 3633328 (NC_000003.11:130189918::TGTG 32/600) Row 3633329 (NC_000003.11:130189918::TGTGTG 1/600)	-	Jul 13, 2019 (153)
87	Northern Sweden Submission ignored due to conflicting rows: Row 3633327 (NC_000003.11:130189918::TG 453/600) Row 3633328 (NC_000003.11:130189918::TGTG 32/600) Row 3633329 (NC_000003.11:130189918::TGTGTG 1/600)	-	Jul 13, 2019 (153)
88	Northern Sweden Submission ignored due to conflicting rows: Row 3633327 (NC_000003.11:130189918::TG 453/600) Row 3633328 (NC_000003.11:130189918::TGTG 32/600) Row 3633329 (NC_000003.11:130189918::TGTGTG 1/600)	-	Jul 13, 2019 (153)
89	8.3KJPN Submission ignored due to conflicting rows: Row 19539997 (NC_000003.11:130189918::TG 6555/16760) Row 19539998 (NC_000003.11:130189918::TGTG 579/16760) Row 19539999 (NC_000003.11:130189918:TGTG: 859/16760)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 19539997 (NC_000003.11:130189918::TG 6555/16760) Row 19539998 (NC_000003.11:130189918::TGTG 579/16760) Row 19539999 (NC_000003.11:130189918:TGTG: 859/16760)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 19539997 (NC_000003.11:130189918::TG 6555/16760) Row 19539998 (NC_000003.11:130189918::TGTG 579/16760) Row 19539999 (NC_000003.11:130189918:TGTG: 859/16760)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 19539997 (NC_000003.11:130189918::TG 6555/16760) Row 19539998 (NC_000003.11:130189918::TGTG 579/16760) Row 19539999 (NC_000003.11:130189918:TGTG: 859/16760)...	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 19539997 (NC_000003.11:130189918::TG 6555/16760) Row 19539998 (NC_000003.11:130189918::TGTG 579/16760) Row 19539999 (NC_000003.11:130189918:TGTG: 859/16760)...	-	Apr 26, 2021 (155)
94	14KJPN Submission ignored due to conflicting rows: Row 28282181 (NC_000003.12:130471074:TGTG: 1453/28258) Row 28282182 (NC_000003.12:130471074::TG 11163/28258) Row 28282183 (NC_000003.12:130471074:TG: 30/28258)...	-	Oct 12, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 28282181 (NC_000003.12:130471074:TGTG: 1453/28258) Row 28282182 (NC_000003.12:130471074::TG 11163/28258) Row 28282183 (NC_000003.12:130471074:TG: 30/28258)...	-	Oct 12, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 28282181 (NC_000003.12:130471074:TGTG: 1453/28258) Row 28282182 (NC_000003.12:130471074::TG 11163/28258) Row 28282183 (NC_000003.12:130471074:TG: 30/28258)...	-	Oct 12, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 28282181 (NC_000003.12:130471074:TGTG: 1453/28258) Row 28282182 (NC_000003.12:130471074::TG 11163/28258) Row 28282183 (NC_000003.12:130471074:TG: 30/28258)...	-	Oct 12, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 28282181 (NC_000003.12:130471074:TGTG: 1453/28258) Row 28282182 (NC_000003.12:130471074::TG 11163/28258) Row 28282183 (NC_000003.12:130471074:TG: 30/28258)...	-	Oct 12, 2022 (156)
99	UK 10K study - Twins Submission ignored due to conflicting rows: Row 9693216 (NC_000003.11:130189918::TG 2573/3708) Row 9693217 (NC_000003.11:130189918::TGTG 184/3708)	-	Oct 12, 2018 (152)
100	UK 10K study - Twins Submission ignored due to conflicting rows: Row 9693216 (NC_000003.11:130189918::TG 2573/3708) Row 9693217 (NC_000003.11:130189918::TGTG 184/3708)	-	Oct 12, 2018 (152)
101	ALFA	NC_000003.12 - 130471075	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)
rs71158195	May 15, 2013 (138)
rs71657090	May 11, 2012 (137)
rs71706828	May 11, 2012 (137)
rs71792655	May 11, 2012 (137)
rs141849400	Sep 17, 2011 (135)
rs377010638	May 13, 2013 (138)
rs796953174	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4080731383	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTG:	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
1940106692	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss4080731382	NC_000003.12:130471074:TGTGTGTGTG:	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	(self)
1940106692	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	(self)
ss4080731381	NC_000003.12:130471074:TGTGTGTG:	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
1940106692	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
ss4080731380	NC_000003.12:130471074:TGTGTG:	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
1940106692	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss288416735	NC_000003.10:131672608:TGTG:	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss2993192447, ss3984446973, ss5161570692	NC_000003.11:130189918:TGTG:	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3710282581, ss4080731379, ss5256015631, ss5455157377, ss5694445077	NC_000003.12:130471074:TGTG:	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
1940106692	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss551376538	NC_000003.10:131672608:TG:	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss1997161963, ss5161570694	NC_000003.11:130189918:TG:	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5848592960	NC_000003.11:130189943:GT:	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT
ss4080731378, ss5455157374, ss5694445079	NC_000003.12:130471074:TG:	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1940106692	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3710282582	NC_000003.12:130471076:TG:	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss326425009, ss326448416, ss551279296, ss553058828	NC_000003.10:131672608::TG	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss288416737	NC_000003.10:131672635::GT	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss663355315, ss666226385, ss1536372586, ss1703822829, ss1703823036, ss3730348462, ss3784463611, ss3789957704, ss3794832272, ss3984262942, ss5161570690, ss5624132315, ss5800109831, ss5826477639, ss5980173762	NC_000003.11:130189918::TG	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss1997161961	NC_000003.11:130189922::TG	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3984262943, ss3984262944	NC_000003.11:130189945::GT	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3064930459, ss4080731373, ss5237178775, ss5256015630, ss5455157373, ss5694445078	NC_000003.12:130471074::TG	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1940106692	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3710282583	NC_000003.12:130471078::TG	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3647526237	NC_000003.12:130471097::GT	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss41971318	NT_005612.16:36685090::TG	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss95331680	NT_005612.16:36685091::GT	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss1703822830, ss1703823037, ss3730348463, ss5161570691, ss5624132314, ss5826477640	NC_000003.11:130189918::TGTG	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4080731374, ss5237178776, ss5256015629, ss5455157375, ss5694445080	NC_000003.12:130471074::TGTG	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1940106692	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3710282584	NC_000003.12:130471078::TGTG	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3730348464, ss5161570693	NC_000003.11:130189918::TGTGTG	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4080731375, ss5455157376, ss5694445081	NC_000003.12:130471074::TGTGTG	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1940106692	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3710282585	NC_000003.12:130471078::TGTGTG	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4080731376	NC_000003.12:130471074::TGTGTGTG	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1940106692	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1940106692	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:130471074:TGTGTGTGTGT… NC_000003.12:130471074:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(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 rs34150957

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
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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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs34150957