Name: rs1157881541
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.

rs1157881541

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:150209919-150209936 (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)₅ / del(A)₄ / delAAA / delAA…
del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA
Variation Type: Indel Insertion and Deletion
Frequency: delAA=0.01704 (220/12912, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ACTR3C : 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	12912	AAAAAAAAAAAAAAAAAA=0.98048	AAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAA=0.01704, AAAAAAAAAAAAAAAAA=0.00178, AAAAAAAAAAAAAAAAAAA=0.00070, AAAAAAAAAAAAAAAAAAAA=0.00000	0.967843	0.002029	0.030128	36
European	Sub	10826	AAAAAAAAAAAAAAAAAA=0.97682	AAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAA=0.02023, AAAAAAAAAAAAAAAAA=0.00212, AAAAAAAAAAAAAAAAAAA=0.00083, AAAAAAAAAAAAAAAAAAAA=0.00000	0.961775	0.002424	0.035801	29
African	Sub	1132	AAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	46	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1086	AAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	64	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	50	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	14	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	100	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	424	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	54	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	312	AAAAAAAAAAAAAAAAAA=0.997	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.003, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	0.99359	0.0	0.00641	0

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	12912	(A)₁₈=0.98048	del(A)₅=0.00000, del(A)₄=0.00000, delAAA=0.00000, delAA=0.01704, delA=0.00178, dupA=0.00070, dupAA=0.00000
Allele Frequency Aggregator	European	Sub	10826	(A)₁₈=0.97682	del(A)₅=0.00000, del(A)₄=0.00000, delAAA=0.00000, delAA=0.02023, delA=0.00212, dupA=0.00083, dupAA=0.00000
Allele Frequency Aggregator	African	Sub	1132	(A)₁₈=1.0000	del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	424	(A)₁₈=1.000	del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	312	(A)₁₈=0.997	del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.003, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	100	(A)₁₈=1.00	del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	64	(A)₁₈=1.00	del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	54	(A)₁₈=1.00	del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 7	NC_000007.14:g.150209932_150209936del
GRCh38.p14 chr 7	NC_000007.14:g.150209933_150209936del
GRCh38.p14 chr 7	NC_000007.14:g.150209934_150209936del
GRCh38.p14 chr 7	NC_000007.14:g.150209935_150209936del
GRCh38.p14 chr 7	NC_000007.14:g.150209936del
GRCh38.p14 chr 7	NC_000007.14:g.150209936dup
GRCh38.p14 chr 7	NC_000007.14:g.150209935_150209936dup
GRCh38.p14 chr 7	NC_000007.14:g.150209934_150209936dup
GRCh37.p13 chr 7	NC_000007.13:g.149907021_149907025del
GRCh37.p13 chr 7	NC_000007.13:g.149907022_149907025del
GRCh37.p13 chr 7	NC_000007.13:g.149907023_149907025del
GRCh37.p13 chr 7	NC_000007.13:g.149907024_149907025del
GRCh37.p13 chr 7	NC_000007.13:g.149907025del
GRCh37.p13 chr 7	NC_000007.13:g.149907025dup
GRCh37.p13 chr 7	NC_000007.13:g.149907024_149907025dup
GRCh37.p13 chr 7	NC_000007.13:g.149907023_149907025dup

Gene: ACTR3C, actin related protein 3C (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ACTR3C transcript variant 4	NM_001351028.2:c.23+74830… NM_001351028.2:c.23+74830_23+74834del	N/A	Intron Variant
ACTR3C transcript variant 5	NM_001351029.2:c.60+10322… NM_001351029.2:c.60+10322_60+10326del	N/A	Intron Variant
ACTR3C transcript variant 6	NM_001351030.2:c.60+10322… NM_001351030.2:c.60+10322_60+10326del	N/A	Intron Variant
ACTR3C transcript variant 3	NM_001351027.2:c.	N/A	Genic Upstream Transcript Variant
ACTR3C transcript variant 1	NM_001164458.2:c.	N/A	Genic Downstream Transcript Variant
ACTR3C transcript variant 2	NM_001164459.2:c.	N/A	Genic Downstream Transcript Variant
ACTR3C transcript variant 7	NR_147012.2:n.	N/A	Intron Variant
ACTR3C transcript variant 9	NR_147014.2:n.	N/A	Intron Variant
ACTR3C transcript variant 10	NR_147015.2:n.	N/A	Intron Variant
ACTR3C transcript variant 11	NR_147016.2:n.	N/A	Intron Variant
ACTR3C transcript variant 12	NR_147017.2:n.	N/A	Intron Variant
ACTR3C transcript variant 13	NR_147018.2:n.	N/A	Intron Variant
ACTR3C transcript variant 14	NR_147019.2:n.	N/A	Intron Variant
ACTR3C transcript variant 15	NR_147020.2:n.	N/A	Genic Upstream Transcript Variant
ACTR3C transcript variant 16	NR_147021.2:n.	N/A	Genic Upstream Transcript Variant
ACTR3C transcript variant 17	NR_147022.2:n.	N/A	Genic Upstream Transcript Variant
ACTR3C transcript variant 8	NR_147013.2:n.	N/A	Genic Downstream Transcript Variant
ACTR3C transcript variant X11	XM_047420749.1:c.564+7483… XM_047420749.1:c.564+74830_564+74834del	N/A	Intron Variant
ACTR3C transcript variant X15	XM_024446884.2:c.	N/A	Genic Upstream Transcript Variant
ACTR3C transcript variant X13	XM_047420750.1:c.	N/A	Genic Upstream Transcript Variant
ACTR3C transcript variant X14	XM_047420751.1:c.	N/A	Genic Upstream Transcript Variant
ACTR3C transcript variant X7	XM_005250043.5:c.	N/A	Genic Downstream Transcript Variant
ACTR3C transcript variant X3	XM_011516506.4:c.	N/A	Genic Downstream Transcript Variant
ACTR3C transcript variant X5	XM_011516507.3:c.	N/A	Genic Downstream Transcript Variant
ACTR3C transcript variant X6	XM_011516508.3:c.	N/A	Genic Downstream Transcript Variant
ACTR3C transcript variant X12	XM_011516511.4:c.	N/A	Genic Downstream Transcript Variant
ACTR3C transcript variant X1	XM_047420748.1:c.	N/A	Genic Downstream Transcript Variant
ACTR3C transcript variant X8	XR_007060143.1:n.	N/A	Intron Variant
ACTR3C transcript variant X9	XR_007060144.1:n.	N/A	Intron Variant
ACTR3C transcript variant X10	XR_007060145.1:n.	N/A	Intron Variant
ACTR3C transcript variant X2	XR_007060141.1:n.	N/A	Genic Downstream Transcript Variant
ACTR3C transcript variant X4	XR_007060142.1:n.	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	(A)₁₈=	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA
GRCh38.p14 chr 7	NC_000007.14:g.150209919_150209936=	NC_000007.14:g.150209932_150209936del	NC_000007.14:g.150209933_150209936del	NC_000007.14:g.150209934_150209936del	NC_000007.14:g.150209935_150209936del	NC_000007.14:g.150209936del	NC_000007.14:g.150209936dup	NC_000007.14:g.150209935_150209936dup	NC_000007.14:g.150209934_150209936dup
GRCh37.p13 chr 7	NC_000007.13:g.149907008_149907025=	NC_000007.13:g.149907021_149907025del	NC_000007.13:g.149907022_149907025del	NC_000007.13:g.149907023_149907025del	NC_000007.13:g.149907024_149907025del	NC_000007.13:g.149907025del	NC_000007.13:g.149907025dup	NC_000007.13:g.149907024_149907025dup	NC_000007.13:g.149907023_149907025dup
ACTR3C transcript variant 4	NM_001351028.2:c.23+74834=	NM_001351028.2:c.23+74830_23+74834del	NM_001351028.2:c.23+74831_23+74834del	NM_001351028.2:c.23+74832_23+74834del	NM_001351028.2:c.23+74833_23+74834del	NM_001351028.2:c.23+74834del	NM_001351028.2:c.23+74834dup	NM_001351028.2:c.23+74833_23+74834dup	NM_001351028.2:c.23+74832_23+74834dup
ACTR3C transcript variant 5	NM_001351029.2:c.60+10326=	NM_001351029.2:c.60+10322_60+10326del	NM_001351029.2:c.60+10323_60+10326del	NM_001351029.2:c.60+10324_60+10326del	NM_001351029.2:c.60+10325_60+10326del	NM_001351029.2:c.60+10326del	NM_001351029.2:c.60+10326dup	NM_001351029.2:c.60+10325_60+10326dup	NM_001351029.2:c.60+10324_60+10326dup
ACTR3C transcript variant 6	NM_001351030.2:c.60+10326=	NM_001351030.2:c.60+10322_60+10326del	NM_001351030.2:c.60+10323_60+10326del	NM_001351030.2:c.60+10324_60+10326del	NM_001351030.2:c.60+10325_60+10326del	NM_001351030.2:c.60+10326del	NM_001351030.2:c.60+10326dup	NM_001351030.2:c.60+10325_60+10326dup	NM_001351030.2:c.60+10324_60+10326dup
ACTR3C transcript variant X11	XM_047420749.1:c.564+74834=	XM_047420749.1:c.564+74830_564+74834del	XM_047420749.1:c.564+74831_564+74834del	XM_047420749.1:c.564+74832_564+74834del	XM_047420749.1:c.564+74833_564+74834del	XM_047420749.1:c.564+74834del	XM_047420749.1:c.564+74834dup	XM_047420749.1:c.564+74833_564+74834dup	XM_047420749.1:c.564+74832_564+74834dup

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#.

39 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SYSTEMSBIOZJU	ss2626882919	Nov 08, 2017 (151)
2	SWEGEN	ss3002286012	Nov 08, 2017 (151)
3	EVA_DECODE	ss3720981700	Jul 13, 2019 (153)
4	EVA_DECODE	ss3720981701	Jul 13, 2019 (153)
5	EVA_DECODE	ss3720981702	Jul 13, 2019 (153)
6	EVA_DECODE	ss3720981703	Jul 13, 2019 (153)
7	ACPOP	ss3735198003	Jul 13, 2019 (153)
8	ACPOP	ss3735198004	Jul 13, 2019 (153)
9	PACBIO	ss3786000289	Jul 13, 2019 (153)
10	PACBIO	ss3791272430	Jul 13, 2019 (153)
11	PACBIO	ss3796152740	Jul 13, 2019 (153)
12	EVA	ss3844405016	Apr 26, 2020 (154)
13	KOGIC	ss3962861366	Apr 26, 2020 (154)
14	KOGIC	ss3962861367	Apr 26, 2020 (154)
15	KOGIC	ss3962861368	Apr 26, 2020 (154)
16	KOGIC	ss3962861369	Apr 26, 2020 (154)
17	GNOMAD	ss4175686234	Apr 26, 2021 (155)
18	GNOMAD	ss4175686235	Apr 26, 2021 (155)
19	GNOMAD	ss4175686236	Apr 26, 2021 (155)
20	GNOMAD	ss4175686237	Apr 26, 2021 (155)
21	GNOMAD	ss4175686238	Apr 26, 2021 (155)
22	GNOMAD	ss4175686239	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5186258937	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5186258938	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5186258939	Apr 26, 2021 (155)
26	1000G_HIGH_COVERAGE	ss5275268069	Oct 16, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5275268070	Oct 16, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5275268071	Oct 16, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5275268072	Oct 16, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5275268073	Oct 16, 2022 (156)
31	HUGCELL_USP	ss5472083280	Oct 16, 2022 (156)
32	HUGCELL_USP	ss5472083282	Oct 16, 2022 (156)
33	HUGCELL_USP	ss5472083283	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5472083284	Oct 16, 2022 (156)
35	TOMMO_GENOMICS	ss5727468453	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5727468454	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5727468455	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5727468457	Oct 16, 2022 (156)
39	EVA	ss5856154827	Oct 16, 2022 (156)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280930205 (NC_000007.14:150209918::A 411/57430) Row 280930206 (NC_000007.14:150209918::AA 1/57558) Row 280930207 (NC_000007.14:150209918::AAA 1/57562)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280930205 (NC_000007.14:150209918::A 411/57430) Row 280930206 (NC_000007.14:150209918::AA 1/57558) Row 280930207 (NC_000007.14:150209918::AAA 1/57562)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280930205 (NC_000007.14:150209918::A 411/57430) Row 280930206 (NC_000007.14:150209918::AA 1/57558) Row 280930207 (NC_000007.14:150209918::AAA 1/57562)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280930205 (NC_000007.14:150209918::A 411/57430) Row 280930206 (NC_000007.14:150209918::AA 1/57558) Row 280930207 (NC_000007.14:150209918::AAA 1/57562)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280930205 (NC_000007.14:150209918::A 411/57430) Row 280930206 (NC_000007.14:150209918::AA 1/57558) Row 280930207 (NC_000007.14:150209918::AAA 1/57562)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280930205 (NC_000007.14:150209918::A 411/57430) Row 280930206 (NC_000007.14:150209918::AA 1/57558) Row 280930207 (NC_000007.14:150209918::AAA 1/57562)...	-	Apr 26, 2021 (155)
46	Korean Genome Project Submission ignored due to conflicting rows: Row 19239367 (NC_000007.14:150209919:AA: 410/1790) Row 19239368 (NC_000007.14:150209921::A 58/1790) Row 19239369 (NC_000007.14:150209920:A: 109/1790)...	-	Apr 26, 2020 (154)
47	Korean Genome Project Submission ignored due to conflicting rows: Row 19239367 (NC_000007.14:150209919:AA: 410/1790) Row 19239368 (NC_000007.14:150209921::A 58/1790) Row 19239369 (NC_000007.14:150209920:A: 109/1790)...	-	Apr 26, 2020 (154)
48	Korean Genome Project Submission ignored due to conflicting rows: Row 19239367 (NC_000007.14:150209919:AA: 410/1790) Row 19239368 (NC_000007.14:150209921::A 58/1790) Row 19239369 (NC_000007.14:150209920:A: 109/1790)...	-	Apr 26, 2020 (154)
49	Korean Genome Project Submission ignored due to conflicting rows: Row 19239367 (NC_000007.14:150209919:AA: 410/1790) Row 19239368 (NC_000007.14:150209921::A 58/1790) Row 19239369 (NC_000007.14:150209920:A: 109/1790)...	-	Apr 26, 2020 (154)
50	Northern Sweden Submission ignored due to conflicting rows: Row 8482868 (NC_000007.13:149907007:AA: 10/582) Row 8482869 (NC_000007.13:149907007:A: 3/582)	-	Jul 13, 2019 (153)
51	Northern Sweden Submission ignored due to conflicting rows: Row 8482868 (NC_000007.13:149907007:AA: 10/582) Row 8482869 (NC_000007.13:149907007:A: 3/582)	-	Jul 13, 2019 (153)
52	8.3KJPN Submission ignored due to conflicting rows: Row 44228244 (NC_000007.13:149907007:AA: 3814/16704) Row 44228245 (NC_000007.13:149907007:A: 38/16704) Row 44228246 (NC_000007.13:149907007::A 13/16704)	-	Apr 26, 2021 (155)
53	8.3KJPN Submission ignored due to conflicting rows: Row 44228244 (NC_000007.13:149907007:AA: 3814/16704) Row 44228245 (NC_000007.13:149907007:A: 38/16704) Row 44228246 (NC_000007.13:149907007::A 13/16704)	-	Apr 26, 2021 (155)
54	8.3KJPN Submission ignored due to conflicting rows: Row 44228244 (NC_000007.13:149907007:AA: 3814/16704) Row 44228245 (NC_000007.13:149907007:A: 38/16704) Row 44228246 (NC_000007.13:149907007::A 13/16704)	-	Apr 26, 2021 (155)
55	14KJPN Submission ignored due to conflicting rows: Row 61305557 (NC_000007.14:150209918:AA: 6806/28248) Row 61305558 (NC_000007.14:150209918:A: 65/28248) Row 61305559 (NC_000007.14:150209918:AAA: 3/28248)...	-	Oct 16, 2022 (156)
56	14KJPN Submission ignored due to conflicting rows: Row 61305557 (NC_000007.14:150209918:AA: 6806/28248) Row 61305558 (NC_000007.14:150209918:A: 65/28248) Row 61305559 (NC_000007.14:150209918:AAA: 3/28248)...	-	Oct 16, 2022 (156)
57	14KJPN Submission ignored due to conflicting rows: Row 61305557 (NC_000007.14:150209918:AA: 6806/28248) Row 61305558 (NC_000007.14:150209918:A: 65/28248) Row 61305559 (NC_000007.14:150209918:AAA: 3/28248)...	-	Oct 16, 2022 (156)
58	14KJPN Submission ignored due to conflicting rows: Row 61305557 (NC_000007.14:150209918:AA: 6806/28248) Row 61305558 (NC_000007.14:150209918:A: 65/28248) Row 61305559 (NC_000007.14:150209918:AAA: 3/28248)...	-	Oct 16, 2022 (156)
59	ALFA	NC_000007.14 - 150209919	Apr 26, 2021 (155)

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

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4175686239	NC_000007.14:150209918:AAAAA:	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
14368254604	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5275268070, ss5472083282	NC_000007.14:150209918:AAAA:	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
14368254604	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3002286012, ss3786000289	NC_000007.13:149907007:AAA:	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3720981703, ss3962861369, ss4175686238, ss5275268073, ss5727468455	NC_000007.14:150209918:AAA:	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
14368254604	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss2626882919, ss3735198003, ss3791272430, ss3796152740, ss5186258937	NC_000007.13:149907007:AA:	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3844405016, ss5275268069, ss5472083283, ss5727468453, ss5856154827	NC_000007.14:150209918:AA:	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
14368254604	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3720981702, ss3962861366	NC_000007.14:150209919:AA:	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3735198004, ss5186258938	NC_000007.13:149907007:A:	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4175686237, ss5275268071, ss5472083280, ss5727468454	NC_000007.14:150209918:A:	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
14368254604	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3720981701, ss3962861368	NC_000007.14:150209920:A:	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5186258939	NC_000007.13:149907007::A	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4175686234, ss5275268072, ss5472083284, ss5727468457	NC_000007.14:150209918::A	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
14368254604	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3720981700, ss3962861367	NC_000007.14:150209921::A	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4175686235	NC_000007.14:150209918::AA	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
14368254604	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4175686236	NC_000007.14:150209918::AAA	NC_000007.14:150209918:AAAAAAAAAAA… NC_000007.14:150209918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(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 rs1157881541

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

rs1157881541