Name: rs34191043
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.

rs34191043

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:70165265-70165285 (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(A)₁₄ / del(A)₁₃ / del(A)₁₂ / d…
del(A)₁₄ / del(A)₁₃ / del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₇ / dup(A)₁₃ / dup(A)₁₅ / dup(A)₂₁ / ins(A)₂₇
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₃=0.000 (0/760, ALFA)
del(A)₁₂=0.000 (0/760, ALFA)
del(A)₁₁=0.000 (0/760, ALFA) (+ 12 more)
del(A)₁₀=0.000 (0/760, ALFA)
del(A)₉=0.000 (0/760, ALFA)
del(A)₈=0.000 (0/760, ALFA)
del(A)₇=0.000 (0/760, ALFA)
del(A)₄=0.000 (0/760, ALFA)
delAAA=0.000 (0/760, ALFA)
delAA=0.000 (0/760, ALFA)
delA=0.000 (0/760, ALFA)
dupA=0.000 (0/760, ALFA)
dupAA=0.000 (0/760, ALFA)
dupAAA=0.000 (0/760, ALFA)
dup(A)₄=0.000 (0/760, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SAR1A : 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	HWEP
Total	Global	760	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
European	Sub	236	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African	Sub	434	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	28	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	406	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	16	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	10	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other Asian	Sub	6	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	18	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	22	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
South Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other	Sub	30	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	760	(A)₂₁=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	African	Sub	434	(A)₂₁=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	European	Sub	236	(A)₂₁=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	30	(A)₂₁=1.00	del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 2	Sub	22	(A)₂₁=1.00	del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	18	(A)₂₁=1.00	del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Asian	Sub	16	(A)₂₁=1.00	del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	4	(A)₂₁=1.0	del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=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 10	NC_000010.11:g.70165272_70165285del
GRCh38.p14 chr 10	NC_000010.11:g.70165273_70165285del
GRCh38.p14 chr 10	NC_000010.11:g.70165274_70165285del
GRCh38.p14 chr 10	NC_000010.11:g.70165275_70165285del
GRCh38.p14 chr 10	NC_000010.11:g.70165276_70165285del
GRCh38.p14 chr 10	NC_000010.11:g.70165277_70165285del
GRCh38.p14 chr 10	NC_000010.11:g.70165278_70165285del
GRCh38.p14 chr 10	NC_000010.11:g.70165279_70165285del
GRCh38.p14 chr 10	NC_000010.11:g.70165281_70165285del
GRCh38.p14 chr 10	NC_000010.11:g.70165282_70165285del
GRCh38.p14 chr 10	NC_000010.11:g.70165283_70165285del
GRCh38.p14 chr 10	NC_000010.11:g.70165284_70165285del
GRCh38.p14 chr 10	NC_000010.11:g.70165285del
GRCh38.p14 chr 10	NC_000010.11:g.70165285dup
GRCh38.p14 chr 10	NC_000010.11:g.70165284_70165285dup
GRCh38.p14 chr 10	NC_000010.11:g.70165283_70165285dup
GRCh38.p14 chr 10	NC_000010.11:g.70165282_70165285dup
GRCh38.p14 chr 10	NC_000010.11:g.70165281_70165285dup
GRCh38.p14 chr 10	NC_000010.11:g.70165279_70165285dup
GRCh38.p14 chr 10	NC_000010.11:g.70165273_70165285dup
GRCh38.p14 chr 10	NC_000010.11:g.70165271_70165285dup
GRCh38.p14 chr 10	NC_000010.11:g.70165265_70165285dup
GRCh38.p14 chr 10	NC_000010.11:g.70165285_70165286insAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 10	NC_000010.10:g.71925028_71925041del
GRCh37.p13 chr 10	NC_000010.10:g.71925029_71925041del
GRCh37.p13 chr 10	NC_000010.10:g.71925030_71925041del
GRCh37.p13 chr 10	NC_000010.10:g.71925031_71925041del
GRCh37.p13 chr 10	NC_000010.10:g.71925032_71925041del
GRCh37.p13 chr 10	NC_000010.10:g.71925033_71925041del
GRCh37.p13 chr 10	NC_000010.10:g.71925034_71925041del
GRCh37.p13 chr 10	NC_000010.10:g.71925035_71925041del
GRCh37.p13 chr 10	NC_000010.10:g.71925037_71925041del
GRCh37.p13 chr 10	NC_000010.10:g.71925038_71925041del
GRCh37.p13 chr 10	NC_000010.10:g.71925039_71925041del
GRCh37.p13 chr 10	NC_000010.10:g.71925040_71925041del
GRCh37.p13 chr 10	NC_000010.10:g.71925041del
GRCh37.p13 chr 10	NC_000010.10:g.71925041dup
GRCh37.p13 chr 10	NC_000010.10:g.71925040_71925041dup
GRCh37.p13 chr 10	NC_000010.10:g.71925039_71925041dup
GRCh37.p13 chr 10	NC_000010.10:g.71925038_71925041dup
GRCh37.p13 chr 10	NC_000010.10:g.71925037_71925041dup
GRCh37.p13 chr 10	NC_000010.10:g.71925035_71925041dup
GRCh37.p13 chr 10	NC_000010.10:g.71925029_71925041dup
GRCh37.p13 chr 10	NC_000010.10:g.71925027_71925041dup
GRCh37.p13 chr 10	NC_000010.10:g.71925021_71925041dup
GRCh37.p13 chr 10	NC_000010.10:g.71925041_71925042insAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: SAR1A, secretion associated Ras related GTPase 1A (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SAR1A transcript variant 1	NM_001142648.2:c.-86-2519… NM_001142648.2:c.-86-2519_-86-2506del	N/A	Intron Variant
SAR1A transcript variant 2	NM_020150.5:c.-16-3347_-1… NM_020150.5:c.-16-3347_-16-3334del	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	(A)₂₁=	del(A)₁₄	del(A)₁₃	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₇	dup(A)₁₃	dup(A)₁₅	dup(A)₂₁	ins(A)₂₇
GRCh38.p14 chr 10	NC_000010.11:g.70165265_70165285=	NC_000010.11:g.70165272_70165285del	NC_000010.11:g.70165273_70165285del	NC_000010.11:g.70165274_70165285del	NC_000010.11:g.70165275_70165285del	NC_000010.11:g.70165276_70165285del	NC_000010.11:g.70165277_70165285del	NC_000010.11:g.70165278_70165285del	NC_000010.11:g.70165279_70165285del	NC_000010.11:g.70165281_70165285del	NC_000010.11:g.70165282_70165285del	NC_000010.11:g.70165283_70165285del	NC_000010.11:g.70165284_70165285del	NC_000010.11:g.70165285del	NC_000010.11:g.70165285dup	NC_000010.11:g.70165284_70165285dup	NC_000010.11:g.70165283_70165285dup	NC_000010.11:g.70165282_70165285dup	NC_000010.11:g.70165281_70165285dup	NC_000010.11:g.70165279_70165285dup	NC_000010.11:g.70165273_70165285dup	NC_000010.11:g.70165271_70165285dup	NC_000010.11:g.70165265_70165285dup	NC_000010.11:g.70165285_70165286insAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 10	NC_000010.10:g.71925021_71925041=	NC_000010.10:g.71925028_71925041del	NC_000010.10:g.71925029_71925041del	NC_000010.10:g.71925030_71925041del	NC_000010.10:g.71925031_71925041del	NC_000010.10:g.71925032_71925041del	NC_000010.10:g.71925033_71925041del	NC_000010.10:g.71925034_71925041del	NC_000010.10:g.71925035_71925041del	NC_000010.10:g.71925037_71925041del	NC_000010.10:g.71925038_71925041del	NC_000010.10:g.71925039_71925041del	NC_000010.10:g.71925040_71925041del	NC_000010.10:g.71925041del	NC_000010.10:g.71925041dup	NC_000010.10:g.71925040_71925041dup	NC_000010.10:g.71925039_71925041dup	NC_000010.10:g.71925038_71925041dup	NC_000010.10:g.71925037_71925041dup	NC_000010.10:g.71925035_71925041dup	NC_000010.10:g.71925029_71925041dup	NC_000010.10:g.71925027_71925041dup	NC_000010.10:g.71925021_71925041dup	NC_000010.10:g.71925041_71925042insAAAAAAAAAAAAAAAAAAAAAAAAAAA
SAR1A transcript variant 1	NM_001142648.1:c.-86-2506=	NM_001142648.1:c.-86-2519_-86-2506del	NM_001142648.1:c.-86-2518_-86-2506del	NM_001142648.1:c.-86-2517_-86-2506del	NM_001142648.1:c.-86-2516_-86-2506del	NM_001142648.1:c.-86-2515_-86-2506del	NM_001142648.1:c.-86-2514_-86-2506del	NM_001142648.1:c.-86-2513_-86-2506del	NM_001142648.1:c.-86-2512_-86-2506del	NM_001142648.1:c.-86-2510_-86-2506del	NM_001142648.1:c.-86-2509_-86-2506del	NM_001142648.1:c.-86-2508_-86-2506del	NM_001142648.1:c.-86-2507_-86-2506del	NM_001142648.1:c.-86-2506del	NM_001142648.1:c.-86-2506dup	NM_001142648.1:c.-86-2507_-86-2506dup	NM_001142648.1:c.-86-2508_-86-2506dup	NM_001142648.1:c.-86-2509_-86-2506dup	NM_001142648.1:c.-86-2510_-86-2506dup	NM_001142648.1:c.-86-2512_-86-2506dup	NM_001142648.1:c.-86-2518_-86-2506dup	NM_001142648.1:c.-86-2520_-86-2506dup	NM_001142648.1:c.-86-2526_-86-2506dup	NM_001142648.1:c.-86-2506_-86-2505insTTTTTTTTTTTTTTTTTTTTTTTTTTT
SAR1A transcript variant 1	NM_001142648.2:c.-86-2506=	NM_001142648.2:c.-86-2519_-86-2506del	NM_001142648.2:c.-86-2518_-86-2506del	NM_001142648.2:c.-86-2517_-86-2506del	NM_001142648.2:c.-86-2516_-86-2506del	NM_001142648.2:c.-86-2515_-86-2506del	NM_001142648.2:c.-86-2514_-86-2506del	NM_001142648.2:c.-86-2513_-86-2506del	NM_001142648.2:c.-86-2512_-86-2506del	NM_001142648.2:c.-86-2510_-86-2506del	NM_001142648.2:c.-86-2509_-86-2506del	NM_001142648.2:c.-86-2508_-86-2506del	NM_001142648.2:c.-86-2507_-86-2506del	NM_001142648.2:c.-86-2506del	NM_001142648.2:c.-86-2506dup	NM_001142648.2:c.-86-2507_-86-2506dup	NM_001142648.2:c.-86-2508_-86-2506dup	NM_001142648.2:c.-86-2509_-86-2506dup	NM_001142648.2:c.-86-2510_-86-2506dup	NM_001142648.2:c.-86-2512_-86-2506dup	NM_001142648.2:c.-86-2518_-86-2506dup	NM_001142648.2:c.-86-2520_-86-2506dup	NM_001142648.2:c.-86-2526_-86-2506dup	NM_001142648.2:c.-86-2506_-86-2505insTTTTTTTTTTTTTTTTTTTTTTTTTTT
SAR1A transcript variant 2	NM_020150.4:c.-16-3334=	NM_020150.4:c.-16-3347_-16-3334del	NM_020150.4:c.-16-3346_-16-3334del	NM_020150.4:c.-16-3345_-16-3334del	NM_020150.4:c.-16-3344_-16-3334del	NM_020150.4:c.-16-3343_-16-3334del	NM_020150.4:c.-16-3342_-16-3334del	NM_020150.4:c.-16-3341_-16-3334del	NM_020150.4:c.-16-3340_-16-3334del	NM_020150.4:c.-16-3338_-16-3334del	NM_020150.4:c.-16-3337_-16-3334del	NM_020150.4:c.-16-3336_-16-3334del	NM_020150.4:c.-16-3335_-16-3334del	NM_020150.4:c.-16-3334del	NM_020150.4:c.-16-3334dup	NM_020150.4:c.-16-3335_-16-3334dup	NM_020150.4:c.-16-3336_-16-3334dup	NM_020150.4:c.-16-3337_-16-3334dup	NM_020150.4:c.-16-3338_-16-3334dup	NM_020150.4:c.-16-3340_-16-3334dup	NM_020150.4:c.-16-3346_-16-3334dup	NM_020150.4:c.-16-3348_-16-3334dup	NM_020150.4:c.-16-3354_-16-3334dup	NM_020150.4:c.-16-3334_-16-3333insTTTTTTTTTTTTTTTTTTTTTTTTTTT
SAR1A transcript variant 2	NM_020150.5:c.-16-3334=	NM_020150.5:c.-16-3347_-16-3334del	NM_020150.5:c.-16-3346_-16-3334del	NM_020150.5:c.-16-3345_-16-3334del	NM_020150.5:c.-16-3344_-16-3334del	NM_020150.5:c.-16-3343_-16-3334del	NM_020150.5:c.-16-3342_-16-3334del	NM_020150.5:c.-16-3341_-16-3334del	NM_020150.5:c.-16-3340_-16-3334del	NM_020150.5:c.-16-3338_-16-3334del	NM_020150.5:c.-16-3337_-16-3334del	NM_020150.5:c.-16-3336_-16-3334del	NM_020150.5:c.-16-3335_-16-3334del	NM_020150.5:c.-16-3334del	NM_020150.5:c.-16-3334dup	NM_020150.5:c.-16-3335_-16-3334dup	NM_020150.5:c.-16-3336_-16-3334dup	NM_020150.5:c.-16-3337_-16-3334dup	NM_020150.5:c.-16-3338_-16-3334dup	NM_020150.5:c.-16-3340_-16-3334dup	NM_020150.5:c.-16-3346_-16-3334dup	NM_020150.5:c.-16-3348_-16-3334dup	NM_020150.5:c.-16-3354_-16-3334dup	NM_020150.5:c.-16-3334_-16-3333insTTTTTTTTTTTTTTTTTTTTTTTTTTT
SAR1A transcript variant X1	XM_005269984.1:c.-16-3334=	XM_005269984.1:c.-16-3347_-16-3334del	XM_005269984.1:c.-16-3346_-16-3334del	XM_005269984.1:c.-16-3345_-16-3334del	XM_005269984.1:c.-16-3344_-16-3334del	XM_005269984.1:c.-16-3343_-16-3334del	XM_005269984.1:c.-16-3342_-16-3334del	XM_005269984.1:c.-16-3341_-16-3334del	XM_005269984.1:c.-16-3340_-16-3334del	XM_005269984.1:c.-16-3338_-16-3334del	XM_005269984.1:c.-16-3337_-16-3334del	XM_005269984.1:c.-16-3336_-16-3334del	XM_005269984.1:c.-16-3335_-16-3334del	XM_005269984.1:c.-16-3334del	XM_005269984.1:c.-16-3334dup	XM_005269984.1:c.-16-3335_-16-3334dup	XM_005269984.1:c.-16-3336_-16-3334dup	XM_005269984.1:c.-16-3337_-16-3334dup	XM_005269984.1:c.-16-3338_-16-3334dup	XM_005269984.1:c.-16-3340_-16-3334dup	XM_005269984.1:c.-16-3346_-16-3334dup	XM_005269984.1:c.-16-3348_-16-3334dup	XM_005269984.1:c.-16-3354_-16-3334dup	XM_005269984.1:c.-16-3334_-16-3333insTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

61 SubSNP, 36 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss39868881	Mar 13, 2006 (126)
2	HGSV	ss80723866	Dec 14, 2007 (129)
3	HGSV	ss82399699	Dec 15, 2007 (130)
4	HUMANGENOME_JCVI	ss95545156	Feb 04, 2009 (130)
5	PJP	ss294663020	May 09, 2011 (144)
6	PJP	ss294663021	May 09, 2011 (144)
7	EVA_UK10K_ALSPAC	ss1706791304	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1706791407	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1710474017	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1710474556	Apr 01, 2015 (144)
11	SWEGEN	ss3006684164	Nov 08, 2017 (151)
12	URBANLAB	ss3649403250	Oct 12, 2018 (152)
13	EVA_DECODE	ss3690127871	Jul 13, 2019 (153)
14	EVA_DECODE	ss3690127872	Jul 13, 2019 (153)
15	EVA_DECODE	ss3690127873	Jul 13, 2019 (153)
16	EVA_DECODE	ss3690127874	Jul 13, 2019 (153)
17	EVA_DECODE	ss3690127875	Jul 13, 2019 (153)
18	ACPOP	ss3737435501	Jul 13, 2019 (153)
19	ACPOP	ss3737435502	Jul 13, 2019 (153)
20	PACBIO	ss3791885136	Jul 13, 2019 (153)
21	PACBIO	ss3791885137	Jul 13, 2019 (153)
22	PACBIO	ss3796767160	Jul 13, 2019 (153)
23	PACBIO	ss3796767161	Jul 13, 2019 (153)
24	EVA	ss3832191932	Apr 26, 2020 (154)
25	GNOMAD	ss4220680269	Apr 26, 2021 (155)
26	GNOMAD	ss4220680270	Apr 26, 2021 (155)
27	GNOMAD	ss4220680271	Apr 26, 2021 (155)
28	GNOMAD	ss4220680272	Apr 26, 2021 (155)
29	GNOMAD	ss4220680273	Apr 26, 2021 (155)
30	GNOMAD	ss4220680274	Apr 26, 2021 (155)
31	GNOMAD	ss4220680275	Apr 26, 2021 (155)
32	GNOMAD	ss4220680276	Apr 26, 2021 (155)
33	GNOMAD	ss4220680277	Apr 26, 2021 (155)
34	GNOMAD	ss4220680278	Apr 26, 2021 (155)
35	GNOMAD	ss4220680279	Apr 26, 2021 (155)
36	GNOMAD	ss4220680280	Apr 26, 2021 (155)
37	GNOMAD	ss4220680281	Apr 26, 2021 (155)
38	GNOMAD	ss4220680282	Apr 26, 2021 (155)
39	GNOMAD	ss4220680283	Apr 26, 2021 (155)
40	GNOMAD	ss4220680284	Apr 26, 2021 (155)
41	GNOMAD	ss4220680285	Apr 26, 2021 (155)
42	GNOMAD	ss4220680286	Apr 26, 2021 (155)
43	GNOMAD	ss4220680287	Apr 26, 2021 (155)
44	GNOMAD	ss4220680288	Apr 26, 2021 (155)
45	GNOMAD	ss4220680289	Apr 26, 2021 (155)
46	GNOMAD	ss4220680290	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5198190971	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5198190972	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5198190973	Apr 26, 2021 (155)
50	1000G_HIGH_COVERAGE	ss5284487674	Oct 16, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5284487675	Oct 16, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5284487677	Oct 16, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5284487678	Oct 16, 2022 (156)
54	HUGCELL_USP	ss5480021681	Oct 16, 2022 (156)
55	HUGCELL_USP	ss5480021682	Oct 16, 2022 (156)
56	HUGCELL_USP	ss5480021683	Oct 16, 2022 (156)
57	HUGCELL_USP	ss5480021684	Oct 16, 2022 (156)
58	TOMMO_GENOMICS	ss5744182655	Oct 16, 2022 (156)
59	TOMMO_GENOMICS	ss5744182656	Oct 16, 2022 (156)
60	TOMMO_GENOMICS	ss5744182658	Oct 16, 2022 (156)
61	EVA	ss5980621955	Oct 16, 2022 (156)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 27944586 (NC_000010.10:71925021:A: 2897/3854) Row 27944587 (NC_000010.10:71925020:AAA: 866/3854)	-	Oct 12, 2018 (152)
63	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 27944586 (NC_000010.10:71925021:A: 2897/3854) Row 27944587 (NC_000010.10:71925020:AAA: 866/3854)	-	Oct 12, 2018 (152)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355795806 (NC_000010.11:70165264::A 1847/84512) Row 355795807 (NC_000010.11:70165264::AA 23/84598) Row 355795808 (NC_000010.11:70165264::AAA 8/84614)...	-	Apr 26, 2021 (155)
87	Northern Sweden Submission ignored due to conflicting rows: Row 10720366 (NC_000010.10:71925020:A: 161/564) Row 10720367 (NC_000010.10:71925020:AA: 164/564)	-	Jul 13, 2019 (153)
88	Northern Sweden Submission ignored due to conflicting rows: Row 10720366 (NC_000010.10:71925020:A: 161/564) Row 10720367 (NC_000010.10:71925020:AA: 164/564)	-	Jul 13, 2019 (153)
89	8.3KJPN Submission ignored due to conflicting rows: Row 56160278 (NC_000010.10:71925020:AA: 949/16480) Row 56160279 (NC_000010.10:71925020:A: 7558/16480) Row 56160280 (NC_000010.10:71925020::A 8/16480)	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 56160278 (NC_000010.10:71925020:AA: 949/16480) Row 56160279 (NC_000010.10:71925020:A: 7558/16480) Row 56160280 (NC_000010.10:71925020::A 8/16480)	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 56160278 (NC_000010.10:71925020:AA: 949/16480) Row 56160279 (NC_000010.10:71925020:A: 7558/16480) Row 56160280 (NC_000010.10:71925020::A 8/16480)	-	Apr 26, 2021 (155)
92	14KJPN Submission ignored due to conflicting rows: Row 78019759 (NC_000010.11:70165264:A: 14497/27844) Row 78019760 (NC_000010.11:70165264:AA: 1704/27844) Row 78019762 (NC_000010.11:70165264::A 10/27844)	-	Oct 16, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 78019759 (NC_000010.11:70165264:A: 14497/27844) Row 78019760 (NC_000010.11:70165264:AA: 1704/27844) Row 78019762 (NC_000010.11:70165264::A 10/27844)	-	Oct 16, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 78019759 (NC_000010.11:70165264:A: 14497/27844) Row 78019760 (NC_000010.11:70165264:AA: 1704/27844) Row 78019762 (NC_000010.11:70165264::A 10/27844)	-	Oct 16, 2022 (156)
95	UK 10K study - Twins Submission ignored due to conflicting rows: Row 27944586 (NC_000010.10:71925021:A: 2848/3708) Row 27944587 (NC_000010.10:71925020:AAA: 763/3708)	-	Oct 12, 2018 (152)
96	UK 10K study - Twins Submission ignored due to conflicting rows: Row 27944586 (NC_000010.10:71925021:A: 2848/3708) Row 27944587 (NC_000010.10:71925020:AAA: 763/3708)	-	Oct 12, 2018 (152)
97	ALFA	NC_000010.11 - 70165265	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)
rs58199348	May 24, 2008 (130)
rs144241912	Jul 01, 2015 (144)
rs149555481	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4220680290	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAA	(self)
ss4220680289	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
4810128606	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
ss4220680288	NC_000010.11:70165264:AAAAAAAAAAAA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
4810128606	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4220680287	NC_000010.11:70165264:AAAAAAAAAAA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
4810128606	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4220680286	NC_000010.11:70165264:AAAAAAAAAA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
4810128606	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4220680285	NC_000010.11:70165264:AAAAAAAAA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
4810128606	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4220680284	NC_000010.11:70165264:AAAAAAAA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
4810128606	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4220680283	NC_000010.11:70165264:AAAAAAA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
4810128606	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3690127875, ss4220680282	NC_000010.11:70165264:AAAAA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4220680281	NC_000010.11:70165264:AAAA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
4810128606	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss1706791304, ss1706791407	NC_000010.10:71925020:AAA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4220680280, ss5284487678, ss5480021681	NC_000010.11:70165264:AAA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
4810128606	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3690127874	NC_000010.11:70165266:AAA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss82399699	NC_000010.8:71595045:AA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss294663020	NC_000010.9:71595026:AA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss294663021	NC_000010.9:71595045:AA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3006684164, ss3737435502, ss3791885136, ss3796767160, ss3832191932, ss5198190971, ss5980621955	NC_000010.10:71925020:AA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss1710474017, ss1710474556	NC_000010.10:71925021:AA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3649403250, ss4220680279, ss5284487674, ss5480021682, ss5744182656	NC_000010.11:70165264:AA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
4810128606	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3690127873	NC_000010.11:70165267:AA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss39868881, ss95545156	NT_030059.13:22729503:AA:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss80723866	NC_000010.8:71595046:A:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3737435501, ss3791885137, ss3796767161, ss5198190972	NC_000010.10:71925020:A:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
	NC_000010.10:71925021:A:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5284487675, ss5480021683, ss5744182655	NC_000010.11:70165264:A:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
4810128606	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3690127872	NC_000010.11:70165268:A:	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5198190973	NC_000010.10:71925020::A	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220680269, ss5284487677, ss5480021684, ss5744182658	NC_000010.11:70165264::A	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
4810128606	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3690127871	NC_000010.11:70165269::A	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220680270	NC_000010.11:70165264::AA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
4810128606	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220680271	NC_000010.11:70165264::AAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
4810128606	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220680272	NC_000010.11:70165264::AAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4810128606	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220680273	NC_000010.11:70165264::AAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220680274	NC_000010.11:70165264::AAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220680275	NC_000010.11:70165264::AAAAAAAAAAA… NC_000010.11:70165264::AAAAAAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220680276	NC_000010.11:70165264::AAAAAAAAAAA… NC_000010.11:70165264::AAAAAAAAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220680277	NC_000010.11:70165264::AAAAAAAAAAA… NC_000010.11:70165264::AAAAAAAAAAAAAAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220680278	NC_000010.11:70165264::AAAAAAAAAAA… NC_000010.11:70165264::AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:70165264:AAAAAAAAAAAA… NC_000010.11:70165264:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs34191043

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

rs34191043