Name: rs150061523
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.

rs150061523

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:139641939-139641957 (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)₁₁ / del(A)₁₀ / del(A)₆ / de…
del(A)₁₁ / del(A)₁₀ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.1152 (808/7012, ALFA)
delA=0.3502 (1754/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: QKILA : 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	7012	AAAAAAAAAAAAAAAAAAA=0.7828	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.1152, AAAAAAAAAAAAAAAAAAAA=0.0575, AAAAAAAAAAAAAAAAAAAAA=0.0426, AAAAAAAAAAAAAAAAAAAAAA=0.0009, AAAAAAAAAAAAAAAAAAAAAAAA=0.0010	0.803363	0.033974	0.162663	32
European	Sub	6058	AAAAAAAAAAAAAAAAAAA=0.7494	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.1327, AAAAAAAAAAAAAAAAAAAA=0.0664, AAAAAAAAAAAAAAAAAAAAA=0.0494, AAAAAAAAAAAAAAAAAAAAAA=0.0010, AAAAAAAAAAAAAAAAAAAAAAAA=0.0012	0.765792	0.040197	0.194011	32
African	Sub	720	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	34	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	686	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	22	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	20	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	2	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	26	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	54	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	26	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	106	AAAAAAAAAAAAAAAAAAA=0.953	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.038, AAAAAAAAAAAAAAAAAAAA=0.009, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	0.961538	0.019231	0.019231	13

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	7012	(A)₁₉=0.7828	del(A)₁₁=0.0000, del(A)₁₀=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.1152, dupA=0.0575, dupAA=0.0426, dupAAA=0.0009, dup(A)₅=0.0010
Allele Frequency Aggregator	European	Sub	6058	(A)₁₉=0.7494	del(A)₁₁=0.0000, del(A)₁₀=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.1327, dupA=0.0664, dupAA=0.0494, dupAAA=0.0010, dup(A)₅=0.0012
Allele Frequency Aggregator	African	Sub	720	(A)₁₉=1.000	del(A)₁₁=0.000, del(A)₁₀=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Other	Sub	106	(A)₁₉=0.953	del(A)₁₁=0.000, del(A)₁₀=0.000, delAAA=0.000, delAA=0.000, delA=0.038, dupA=0.009, dupAA=0.000, dupAAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	54	(A)₁₉=1.00	del(A)₁₁=0.00, del(A)₁₀=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	26	(A)₁₉=1.00	del(A)₁₁=0.00, del(A)₁₀=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	26	(A)₁₉=1.00	del(A)₁₁=0.00, del(A)₁₀=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Asian	Sub	22	(A)₁₉=1.00	del(A)₁₁=0.00, del(A)₁₀=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=0.00
1000Genomes	Global	Study-wide	5008	(A)₁₉=0.6498	delA=0.3502
1000Genomes	African	Sub	1322	(A)₁₉=0.7239	delA=0.2761
1000Genomes	East Asian	Sub	1008	(A)₁₉=0.6905	delA=0.3095
1000Genomes	Europe	Sub	1006	(A)₁₉=0.6342	delA=0.3658
1000Genomes	South Asian	Sub	978	(A)₁₉=0.638	delA=0.362
1000Genomes	American	Sub	694	(A)₁₉=0.488	delA=0.512

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 4	NC_000004.12:g.139641947_139641957del
GRCh38.p14 chr 4	NC_000004.12:g.139641948_139641957del
GRCh38.p14 chr 4	NC_000004.12:g.139641952_139641957del
GRCh38.p14 chr 4	NC_000004.12:g.139641953_139641957del
GRCh38.p14 chr 4	NC_000004.12:g.139641954_139641957del
GRCh38.p14 chr 4	NC_000004.12:g.139641955_139641957del
GRCh38.p14 chr 4	NC_000004.12:g.139641956_139641957del
GRCh38.p14 chr 4	NC_000004.12:g.139641957del
GRCh38.p14 chr 4	NC_000004.12:g.139641957dup
GRCh38.p14 chr 4	NC_000004.12:g.139641956_139641957dup
GRCh38.p14 chr 4	NC_000004.12:g.139641955_139641957dup
GRCh38.p14 chr 4	NC_000004.12:g.139641954_139641957dup
GRCh38.p14 chr 4	NC_000004.12:g.139641953_139641957dup
GRCh37.p13 chr 4	NC_000004.11:g.140563101_140563111del
GRCh37.p13 chr 4	NC_000004.11:g.140563102_140563111del
GRCh37.p13 chr 4	NC_000004.11:g.140563106_140563111del
GRCh37.p13 chr 4	NC_000004.11:g.140563107_140563111del
GRCh37.p13 chr 4	NC_000004.11:g.140563108_140563111del
GRCh37.p13 chr 4	NC_000004.11:g.140563109_140563111del
GRCh37.p13 chr 4	NC_000004.11:g.140563110_140563111del
GRCh37.p13 chr 4	NC_000004.11:g.140563111del
GRCh37.p13 chr 4	NC_000004.11:g.140563111dup
GRCh37.p13 chr 4	NC_000004.11:g.140563110_140563111dup
GRCh37.p13 chr 4	NC_000004.11:g.140563109_140563111dup
GRCh37.p13 chr 4	NC_000004.11:g.140563108_140563111dup
GRCh37.p13 chr 4	NC_000004.11:g.140563107_140563111dup

Gene: QKILA, uncharacterized QKILA (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
QKILA transcript	XR_939252.3:n.	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)₁₉=	del(A)₁₁	del(A)₁₀	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅
GRCh38.p14 chr 4	NC_000004.12:g.139641939_139641957=	NC_000004.12:g.139641947_139641957del	NC_000004.12:g.139641948_139641957del	NC_000004.12:g.139641952_139641957del	NC_000004.12:g.139641953_139641957del	NC_000004.12:g.139641954_139641957del	NC_000004.12:g.139641955_139641957del	NC_000004.12:g.139641956_139641957del	NC_000004.12:g.139641957del	NC_000004.12:g.139641957dup	NC_000004.12:g.139641956_139641957dup	NC_000004.12:g.139641955_139641957dup	NC_000004.12:g.139641954_139641957dup	NC_000004.12:g.139641953_139641957dup
GRCh37.p13 chr 4	NC_000004.11:g.140563093_140563111=	NC_000004.11:g.140563101_140563111del	NC_000004.11:g.140563102_140563111del	NC_000004.11:g.140563106_140563111del	NC_000004.11:g.140563107_140563111del	NC_000004.11:g.140563108_140563111del	NC_000004.11:g.140563109_140563111del	NC_000004.11:g.140563110_140563111del	NC_000004.11:g.140563111del	NC_000004.11:g.140563111dup	NC_000004.11:g.140563110_140563111dup	NC_000004.11:g.140563109_140563111dup	NC_000004.11:g.140563108_140563111dup	NC_000004.11:g.140563107_140563111dup

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#.

40 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PJP	ss295191077	May 09, 2011 (134)
2	BILGI_BIOE	ss666281051	Apr 25, 2013 (138)
3	1000GENOMES	ss1372867648	Aug 21, 2014 (142)
4	SWEGEN	ss2995671172	Nov 08, 2017 (151)
5	ACPOP	ss3731672033	Jul 13, 2019 (153)
6	ACPOP	ss3731672034	Jul 13, 2019 (153)
7	ACPOP	ss3731672035	Jul 13, 2019 (153)
8	KHV_HUMAN_GENOMES	ss3805658306	Jul 13, 2019 (153)
9	EVA	ss3828846405	Apr 26, 2020 (154)
10	GNOMAD	ss4121644088	Apr 26, 2021 (155)
11	GNOMAD	ss4121644089	Apr 26, 2021 (155)
12	GNOMAD	ss4121644090	Apr 26, 2021 (155)
13	GNOMAD	ss4121644091	Apr 26, 2021 (155)
14	GNOMAD	ss4121644092	Apr 26, 2021 (155)
15	GNOMAD	ss4121644093	Apr 26, 2021 (155)
16	GNOMAD	ss4121644094	Apr 26, 2021 (155)
17	GNOMAD	ss4121644095	Apr 26, 2021 (155)
18	GNOMAD	ss4121644096	Apr 26, 2021 (155)
19	GNOMAD	ss4121644097	Apr 26, 2021 (155)
20	GNOMAD	ss4121644098	Apr 26, 2021 (155)
21	GNOMAD	ss4121644099	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5168322398	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5168322399	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5168322400	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5168322401	Apr 26, 2021 (155)
26	1000G_HIGH_COVERAGE	ss5261267571	Oct 13, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5261267572	Oct 13, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5261267573	Oct 13, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5261267574	Oct 13, 2022 (156)
30	HUGCELL_USP	ss5459800568	Oct 13, 2022 (156)
31	HUGCELL_USP	ss5459800569	Oct 13, 2022 (156)
32	HUGCELL_USP	ss5459800570	Oct 13, 2022 (156)
33	HUGCELL_USP	ss5459800571	Oct 13, 2022 (156)
34	TOMMO_GENOMICS	ss5703401225	Oct 13, 2022 (156)
35	TOMMO_GENOMICS	ss5703401226	Oct 13, 2022 (156)
36	TOMMO_GENOMICS	ss5703401227	Oct 13, 2022 (156)
37	TOMMO_GENOMICS	ss5703401228	Oct 13, 2022 (156)
38	TOMMO_GENOMICS	ss5703401229	Oct 13, 2022 (156)
39	EVA	ss5844810494	Oct 13, 2022 (156)
40	EVA	ss5844810495	Oct 13, 2022 (156)
41	1000Genomes	NC_000004.11 - 140563093	Oct 12, 2018 (152)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 167027496 (NC_000004.12:139641938::A 17351/112212) Row 167027497 (NC_000004.12:139641938::AA 7765/112194) Row 167027498 (NC_000004.12:139641938::AAA 15/112326)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 167027496 (NC_000004.12:139641938::A 17351/112212) Row 167027497 (NC_000004.12:139641938::AA 7765/112194) Row 167027498 (NC_000004.12:139641938::AAA 15/112326)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 167027496 (NC_000004.12:139641938::A 17351/112212) Row 167027497 (NC_000004.12:139641938::AA 7765/112194) Row 167027498 (NC_000004.12:139641938::AAA 15/112326)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 167027496 (NC_000004.12:139641938::A 17351/112212) Row 167027497 (NC_000004.12:139641938::AA 7765/112194) Row 167027498 (NC_000004.12:139641938::AAA 15/112326)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 167027496 (NC_000004.12:139641938::A 17351/112212) Row 167027497 (NC_000004.12:139641938::AA 7765/112194) Row 167027498 (NC_000004.12:139641938::AAA 15/112326)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 167027496 (NC_000004.12:139641938::A 17351/112212) Row 167027497 (NC_000004.12:139641938::AA 7765/112194) Row 167027498 (NC_000004.12:139641938::AAA 15/112326)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 167027496 (NC_000004.12:139641938::A 17351/112212) Row 167027497 (NC_000004.12:139641938::AA 7765/112194) Row 167027498 (NC_000004.12:139641938::AAA 15/112326)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 167027496 (NC_000004.12:139641938::A 17351/112212) Row 167027497 (NC_000004.12:139641938::AA 7765/112194) Row 167027498 (NC_000004.12:139641938::AAA 15/112326)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 167027496 (NC_000004.12:139641938::A 17351/112212) Row 167027497 (NC_000004.12:139641938::AA 7765/112194) Row 167027498 (NC_000004.12:139641938::AAA 15/112326)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 167027496 (NC_000004.12:139641938::A 17351/112212) Row 167027497 (NC_000004.12:139641938::AA 7765/112194) Row 167027498 (NC_000004.12:139641938::AAA 15/112326)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 167027496 (NC_000004.12:139641938::A 17351/112212) Row 167027497 (NC_000004.12:139641938::AA 7765/112194) Row 167027498 (NC_000004.12:139641938::AAA 15/112326)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 167027496 (NC_000004.12:139641938::A 17351/112212) Row 167027497 (NC_000004.12:139641938::AA 7765/112194) Row 167027498 (NC_000004.12:139641938::AAA 15/112326)...	-	Apr 26, 2021 (155)
54	Northern Sweden Submission ignored due to conflicting rows: Row 4956898 (NC_000004.11:140563092::A 51/504) Row 4956899 (NC_000004.11:140563092:A: 133/504) Row 4956900 (NC_000004.11:140563092::AA 29/504)	-	Jul 13, 2019 (153)
55	Northern Sweden Submission ignored due to conflicting rows: Row 4956898 (NC_000004.11:140563092::A 51/504) Row 4956899 (NC_000004.11:140563092:A: 133/504) Row 4956900 (NC_000004.11:140563092::AA 29/504)	-	Jul 13, 2019 (153)
56	Northern Sweden Submission ignored due to conflicting rows: Row 4956898 (NC_000004.11:140563092::A 51/504) Row 4956899 (NC_000004.11:140563092:A: 133/504) Row 4956900 (NC_000004.11:140563092::AA 29/504)	-	Jul 13, 2019 (153)
57	8.3KJPN Submission ignored due to conflicting rows: Row 26291705 (NC_000004.11:140563092:A: 4546/16602) Row 26291706 (NC_000004.11:140563092::A 1630/16602) Row 26291707 (NC_000004.11:140563092::AA 867/16602)...	-	Apr 26, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 26291705 (NC_000004.11:140563092:A: 4546/16602) Row 26291706 (NC_000004.11:140563092::A 1630/16602) Row 26291707 (NC_000004.11:140563092::AA 867/16602)...	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 26291705 (NC_000004.11:140563092:A: 4546/16602) Row 26291706 (NC_000004.11:140563092::A 1630/16602) Row 26291707 (NC_000004.11:140563092::AA 867/16602)...	-	Apr 26, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 26291705 (NC_000004.11:140563092:A: 4546/16602) Row 26291706 (NC_000004.11:140563092::A 1630/16602) Row 26291707 (NC_000004.11:140563092::AA 867/16602)...	-	Apr 26, 2021 (155)
61	14KJPN Submission ignored due to conflicting rows: Row 37238329 (NC_000004.12:139641938::A 2867/28180) Row 37238330 (NC_000004.12:139641938:A: 8471/28180) Row 37238331 (NC_000004.12:139641938::AA 1546/28180)...	-	Oct 13, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 37238329 (NC_000004.12:139641938::A 2867/28180) Row 37238330 (NC_000004.12:139641938:A: 8471/28180) Row 37238331 (NC_000004.12:139641938::AA 1546/28180)...	-	Oct 13, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 37238329 (NC_000004.12:139641938::A 2867/28180) Row 37238330 (NC_000004.12:139641938:A: 8471/28180) Row 37238331 (NC_000004.12:139641938::AA 1546/28180)...	-	Oct 13, 2022 (156)
64	14KJPN Submission ignored due to conflicting rows: Row 37238329 (NC_000004.12:139641938::A 2867/28180) Row 37238330 (NC_000004.12:139641938:A: 8471/28180) Row 37238331 (NC_000004.12:139641938::AA 1546/28180)...	-	Oct 13, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 37238329 (NC_000004.12:139641938::A 2867/28180) Row 37238330 (NC_000004.12:139641938:A: 8471/28180) Row 37238331 (NC_000004.12:139641938::AA 1546/28180)...	-	Oct 13, 2022 (156)
66	ALFA	NC_000004.12 - 139641939	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
ss4121644099	NC_000004.12:139641938:AAAAAAAAAAA:	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
1636429050	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAA	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
1636429050	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4121644098	NC_000004.12:139641938:AAAAAA:	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4121644097	NC_000004.12:139641938:AAAAA:	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4121644096	NC_000004.12:139641938:AAAA:	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4121644095	NC_000004.12:139641938:AAA:	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
1636429050	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5168322401, ss5844810495	NC_000004.11:140563092:AA:	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4121644094, ss5459800570, ss5703401228	NC_000004.12:139641938:AA:	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
1636429050	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
23581039, ss1372867648, ss2995671172, ss3731672034, ss3828846405, ss5168322398, ss5844810494	NC_000004.11:140563092:A:	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3805658306, ss4121644093, ss5261267572, ss5459800568, ss5703401226	NC_000004.12:139641938:A:	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
1636429050	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss295191077	NC_000004.10:140782543::A	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3731672033, ss5168322399	NC_000004.11:140563092::A	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4121644088, ss5261267573, ss5459800569, ss5703401225	NC_000004.12:139641938::A	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
1636429050	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss666281051, ss3731672035, ss5168322400	NC_000004.11:140563092::AA	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4121644089, ss5261267571, ss5459800571, ss5703401227	NC_000004.12:139641938::AA	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
1636429050	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4121644090, ss5261267574	NC_000004.12:139641938::AAA	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
1636429050	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4121644091	NC_000004.12:139641938::AAAA	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4121644092, ss5703401229	NC_000004.12:139641938::AAAAA	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
1636429050	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000004.12:139641938:AAAAAAAAAAA… NC_000004.12:139641938:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(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 rs150061523

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

rs150061523