Name: rs71574184
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.

rs71574184

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:16416681-16416695 (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)₄ / delAAA / delAA / delA / …
del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₇
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₅=0.4409 (2208/5008, 1000G)
delAAA=0.0000 (0/1844, ALFA)
delAA=0.0000 (0/1844, ALFA) (+ 4 more)
delA=0.0000 (0/1844, ALFA)
dupA=0.0000 (0/1844, ALFA)
dupAA=0.0000 (0/1844, ALFA)
dupAAA=0.0000 (0/1844, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SPATA21 : 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	1844	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
European	Sub	922	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	660	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	32	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	628	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	0	AAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	22	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	128	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	26	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	86	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	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
1000Genomes	Global	Study-wide	5008	(A)₁₅=0.4409	delA=0.5591
1000Genomes	African	Sub	1322	(A)₁₅=0.5560	delA=0.4440
1000Genomes	East Asian	Sub	1008	(A)₁₅=0.1319	delA=0.8681
1000Genomes	Europe	Sub	1006	(A)₁₅=0.3748	delA=0.6252
1000Genomes	South Asian	Sub	978	(A)₁₅=0.612	delA=0.388
1000Genomes	American	Sub	694	(A)₁₅=0.524	delA=0.476
Allele Frequency Aggregator	Total	Global	1844	(A)₁₅=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	922	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	African	Sub	660	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	128	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Other	Sub	86	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	26	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	22	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Asian	Sub	0	(A)₁₅=0	delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=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 1	NC_000001.11:g.16416692_16416695del
GRCh38.p14 chr 1	NC_000001.11:g.16416693_16416695del
GRCh38.p14 chr 1	NC_000001.11:g.16416694_16416695del
GRCh38.p14 chr 1	NC_000001.11:g.16416695del
GRCh38.p14 chr 1	NC_000001.11:g.16416695dup
GRCh38.p14 chr 1	NC_000001.11:g.16416694_16416695dup
GRCh38.p14 chr 1	NC_000001.11:g.16416693_16416695dup
GRCh38.p14 chr 1	NC_000001.11:g.16416689_16416695dup
GRCh37.p13 chr 1	NC_000001.10:g.16743187_16743190del
GRCh37.p13 chr 1	NC_000001.10:g.16743188_16743190del
GRCh37.p13 chr 1	NC_000001.10:g.16743189_16743190del
GRCh37.p13 chr 1	NC_000001.10:g.16743190del
GRCh37.p13 chr 1	NC_000001.10:g.16743190dup
GRCh37.p13 chr 1	NC_000001.10:g.16743189_16743190dup
GRCh37.p13 chr 1	NC_000001.10:g.16743188_16743190dup
GRCh37.p13 chr 1	NC_000001.10:g.16743184_16743190dup
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.220820_220823del
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.220821_220823del
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.220822_220823del
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.220823del
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.220823dup
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.220822_220823dup
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.220821_220823dup
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.220817_220823dup

Gene: SPATA21, spermatogenesis associated 21 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SPATA21 transcript variant 2	NM_001353349.1:c.-63-5769… NM_001353349.1:c.-63-5769_-63-5766del	N/A	Intron Variant
SPATA21 transcript variant 1	NM_198546.1:c.144+4825_14… NM_198546.1:c.144+4825_144+4828del	N/A	Intron Variant
SPATA21 transcript variant 3	NR_148413.2:n.	N/A	Intron Variant
SPATA21 transcript variant X1	XM_011541407.4:c.822+4825… XM_011541407.4:c.822+4825_822+4828del	N/A	Intron Variant
SPATA21 transcript variant X6	XM_011541417.3:c.822+4825… XM_011541417.3:c.822+4825_822+4828del	N/A	Intron Variant
SPATA21 transcript variant X3	XM_017001218.2:c.822+4825… XM_017001218.2:c.822+4825_822+4828del	N/A	Intron Variant
SPATA21 transcript variant X7	XM_047419694.1:c.	N/A	Genic Upstream Transcript Variant
SPATA21 transcript variant X2	XR_001737156.2:n.	N/A	Intron Variant
SPATA21 transcript variant X4	XR_946645.2:n.	N/A	Intron Variant
SPATA21 transcript variant X5	XR_946646.4: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)₁₅=	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₇
GRCh38.p14 chr 1	NC_000001.11:g.16416681_16416695=	NC_000001.11:g.16416692_16416695del	NC_000001.11:g.16416693_16416695del	NC_000001.11:g.16416694_16416695del	NC_000001.11:g.16416695del	NC_000001.11:g.16416695dup	NC_000001.11:g.16416694_16416695dup	NC_000001.11:g.16416693_16416695dup	NC_000001.11:g.16416689_16416695dup
GRCh37.p13 chr 1	NC_000001.10:g.16743176_16743190=	NC_000001.10:g.16743187_16743190del	NC_000001.10:g.16743188_16743190del	NC_000001.10:g.16743189_16743190del	NC_000001.10:g.16743190del	NC_000001.10:g.16743190dup	NC_000001.10:g.16743189_16743190dup	NC_000001.10:g.16743188_16743190dup	NC_000001.10:g.16743184_16743190dup
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.220809_220823=	NW_025791756.1:g.220820_220823del	NW_025791756.1:g.220821_220823del	NW_025791756.1:g.220822_220823del	NW_025791756.1:g.220823del	NW_025791756.1:g.220823dup	NW_025791756.1:g.220822_220823dup	NW_025791756.1:g.220821_220823dup	NW_025791756.1:g.220817_220823dup
SPATA21 transcript variant 2	NM_001353349.1:c.-63-5766=	NM_001353349.1:c.-63-5769_-63-5766del	NM_001353349.1:c.-63-5768_-63-5766del	NM_001353349.1:c.-63-5767_-63-5766del	NM_001353349.1:c.-63-5766del	NM_001353349.1:c.-63-5766dup	NM_001353349.1:c.-63-5767_-63-5766dup	NM_001353349.1:c.-63-5768_-63-5766dup	NM_001353349.1:c.-63-5772_-63-5766dup
SPATA21 transcript variant 1	NM_198546.1:c.144+4828=	NM_198546.1:c.144+4825_144+4828del	NM_198546.1:c.144+4826_144+4828del	NM_198546.1:c.144+4827_144+4828del	NM_198546.1:c.144+4828del	NM_198546.1:c.144+4828dup	NM_198546.1:c.144+4827_144+4828dup	NM_198546.1:c.144+4826_144+4828dup	NM_198546.1:c.144+4822_144+4828dup
SPATA21 transcript variant X1	XM_005245866.1:c.-63-5766=	XM_005245866.1:c.-63-5769_-63-5766del	XM_005245866.1:c.-63-5768_-63-5766del	XM_005245866.1:c.-63-5767_-63-5766del	XM_005245866.1:c.-63-5766del	XM_005245866.1:c.-63-5766dup	XM_005245866.1:c.-63-5767_-63-5766dup	XM_005245866.1:c.-63-5768_-63-5766dup	XM_005245866.1:c.-63-5772_-63-5766dup
SPATA21 transcript variant X1	XM_011541407.4:c.822+4828=	XM_011541407.4:c.822+4825_822+4828del	XM_011541407.4:c.822+4826_822+4828del	XM_011541407.4:c.822+4827_822+4828del	XM_011541407.4:c.822+4828del	XM_011541407.4:c.822+4828dup	XM_011541407.4:c.822+4827_822+4828dup	XM_011541407.4:c.822+4826_822+4828dup	XM_011541407.4:c.822+4822_822+4828dup
SPATA21 transcript variant X6	XM_011541417.3:c.822+4828=	XM_011541417.3:c.822+4825_822+4828del	XM_011541417.3:c.822+4826_822+4828del	XM_011541417.3:c.822+4827_822+4828del	XM_011541417.3:c.822+4828del	XM_011541417.3:c.822+4828dup	XM_011541417.3:c.822+4827_822+4828dup	XM_011541417.3:c.822+4826_822+4828dup	XM_011541417.3:c.822+4822_822+4828dup
SPATA21 transcript variant X3	XM_017001218.2:c.822+4828=	XM_017001218.2:c.822+4825_822+4828del	XM_017001218.2:c.822+4826_822+4828del	XM_017001218.2:c.822+4827_822+4828del	XM_017001218.2:c.822+4828del	XM_017001218.2:c.822+4828dup	XM_017001218.2:c.822+4827_822+4828dup	XM_017001218.2:c.822+4826_822+4828dup	XM_017001218.2:c.822+4822_822+4828dup

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#.

43 SubSNP, 14 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss98567297	Feb 13, 2009 (130)
2	BUSHMAN	ss193088870	Jul 04, 2010 (132)
3	GMI	ss287953061	May 04, 2012 (137)
4	PJP	ss294567370	May 09, 2011 (137)
5	1000GENOMES	ss1367664977	Aug 21, 2014 (142)
6	HAMMER_LAB	ss1793970826	Sep 08, 2015 (146)
7	SYSTEMSBIOZJU	ss2624297093	Nov 08, 2017 (151)
8	SWEGEN	ss2986369592	Nov 08, 2017 (151)
9	MCHAISSO	ss3063578497	Nov 08, 2017 (151)
10	MCHAISSO	ss3064391318	Nov 08, 2017 (151)
11	MCHAISSO	ss3065289080	Nov 08, 2017 (151)
12	BIOINF_KMB_FNS_UNIBA	ss3645028894	Oct 11, 2018 (152)
13	URBANLAB	ss3646609008	Oct 11, 2018 (152)
14	EVA_DECODE	ss3686240853	Jul 12, 2019 (153)
15	EVA_DECODE	ss3686240854	Jul 12, 2019 (153)
16	EVA_DECODE	ss3686240855	Jul 12, 2019 (153)
17	EVA_DECODE	ss3686240856	Jul 12, 2019 (153)
18	EVA_DECODE	ss3686240857	Jul 12, 2019 (153)
19	PACBIO	ss3783335021	Jul 12, 2019 (153)
20	PACBIO	ss3789007661	Jul 12, 2019 (153)
21	PACBIO	ss3793880394	Jul 12, 2019 (153)
22	KHV_HUMAN_GENOMES	ss3798897352	Jul 12, 2019 (153)
23	EVA	ss3826042753	Apr 25, 2020 (154)
24	GNOMAD	ss3988984032	Apr 27, 2021 (155)
25	GNOMAD	ss3988984033	Apr 27, 2021 (155)
26	GNOMAD	ss3988984034	Apr 27, 2021 (155)
27	GNOMAD	ss3988984035	Apr 27, 2021 (155)
28	GNOMAD	ss3988984036	Apr 27, 2021 (155)
29	GNOMAD	ss3988984037	Apr 27, 2021 (155)
30	TOMMO_GENOMICS	ss5142667549	Apr 27, 2021 (155)
31	TOMMO_GENOMICS	ss5142667550	Apr 27, 2021 (155)
32	TOMMO_GENOMICS	ss5142667551	Apr 27, 2021 (155)
33	1000G_HIGH_COVERAGE	ss5241322435	Oct 12, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5241322436	Oct 12, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5241322437	Oct 12, 2022 (156)
36	HUGCELL_USP	ss5442499729	Oct 12, 2022 (156)
37	HUGCELL_USP	ss5442499730	Oct 12, 2022 (156)
38	HUGCELL_USP	ss5442499731	Oct 12, 2022 (156)
39	TOMMO_GENOMICS	ss5667035354	Oct 12, 2022 (156)
40	TOMMO_GENOMICS	ss5667035355	Oct 12, 2022 (156)
41	TOMMO_GENOMICS	ss5667035356	Oct 12, 2022 (156)
42	EVA	ss5831592933	Oct 12, 2022 (156)
43	EVA	ss5848800672	Oct 12, 2022 (156)
44	1000Genomes	NC_000001.10 - 16743176	Oct 11, 2018 (152)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3583133 (NC_000001.11:16416680::A 194/119692) Row 3583134 (NC_000001.11:16416680::AA 6/119714) Row 3583135 (NC_000001.11:16416680:A: 75709/119506)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3583133 (NC_000001.11:16416680::A 194/119692) Row 3583134 (NC_000001.11:16416680::AA 6/119714) Row 3583135 (NC_000001.11:16416680:A: 75709/119506)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3583133 (NC_000001.11:16416680::A 194/119692) Row 3583134 (NC_000001.11:16416680::AA 6/119714) Row 3583135 (NC_000001.11:16416680:A: 75709/119506)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3583133 (NC_000001.11:16416680::A 194/119692) Row 3583134 (NC_000001.11:16416680::AA 6/119714) Row 3583135 (NC_000001.11:16416680:A: 75709/119506)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3583133 (NC_000001.11:16416680::A 194/119692) Row 3583134 (NC_000001.11:16416680::AA 6/119714) Row 3583135 (NC_000001.11:16416680:A: 75709/119506)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3583133 (NC_000001.11:16416680::A 194/119692) Row 3583134 (NC_000001.11:16416680::AA 6/119714) Row 3583135 (NC_000001.11:16416680:A: 75709/119506)...	-	Apr 27, 2021 (155)
51	8.3KJPN Submission ignored due to conflicting rows: Row 636856 (NC_000001.10:16743175:A: 15677/16696) Row 636857 (NC_000001.10:16743175:AA: 25/16696) Row 636858 (NC_000001.10:16743175::A 2/16696)	-	Apr 27, 2021 (155)
52	8.3KJPN Submission ignored due to conflicting rows: Row 636856 (NC_000001.10:16743175:A: 15677/16696) Row 636857 (NC_000001.10:16743175:AA: 25/16696) Row 636858 (NC_000001.10:16743175::A 2/16696)	-	Apr 27, 2021 (155)
53	8.3KJPN Submission ignored due to conflicting rows: Row 636856 (NC_000001.10:16743175:A: 15677/16696) Row 636857 (NC_000001.10:16743175:AA: 25/16696) Row 636858 (NC_000001.10:16743175::A 2/16696)	-	Apr 27, 2021 (155)
54	14KJPN Submission ignored due to conflicting rows: Row 872458 (NC_000001.11:16416680:A: 26605/28240) Row 872459 (NC_000001.11:16416680:AA: 32/28240) Row 872460 (NC_000001.11:16416680::A 3/28240)	-	Oct 12, 2022 (156)
55	14KJPN Submission ignored due to conflicting rows: Row 872458 (NC_000001.11:16416680:A: 26605/28240) Row 872459 (NC_000001.11:16416680:AA: 32/28240) Row 872460 (NC_000001.11:16416680::A 3/28240)	-	Oct 12, 2022 (156)
56	14KJPN Submission ignored due to conflicting rows: Row 872458 (NC_000001.11:16416680:A: 26605/28240) Row 872459 (NC_000001.11:16416680:AA: 32/28240) Row 872460 (NC_000001.11:16416680::A 3/28240)	-	Oct 12, 2022 (156)
57	ALFA	NC_000001.11 - 16416681	Apr 27, 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)
rs138373285	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3988984037	NC_000001.11:16416680:AAAA:	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3686240857, ss3988984036	NC_000001.11:16416680:AAA:	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
9182202226	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss5142667550	NC_000001.10:16743175:AA:	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3988984035, ss5241322436, ss5442499729, ss5667035355	NC_000001.11:16416680:AA:	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
9182202226	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3686240856	NC_000001.11:16416681:AA:	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss287953061	NC_000001.9:16615762:A:	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss294567370	NC_000001.9:16615776:A:	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
512977, ss1367664977, ss1793970826, ss2624297093, ss2986369592, ss3783335021, ss3789007661, ss3793880394, ss3826042753, ss5142667549, ss5831592933	NC_000001.10:16743175:A:	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3063578497, ss3064391318, ss3065289080, ss3645028894, ss3646609008, ss3798897352, ss3988984034, ss5241322435, ss5442499730, ss5667035354, ss5848800672	NC_000001.11:16416680:A:	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
9182202226	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3686240855	NC_000001.11:16416682:A:	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss98567297	NT_004610.19:3423263:A:	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss193088870	NT_032977.10:15830692:A:	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5142667551	NC_000001.10:16743175::A	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3988984032, ss5241322437, ss5442499731, ss5667035356	NC_000001.11:16416680::A	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
9182202226	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3686240854	NC_000001.11:16416683::A	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3988984033	NC_000001.11:16416680::AA	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
9182202226	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
9182202226	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3686240853	NC_000001.11:16416683::AAAAAAA	NC_000001.11:16416680:AAAAAAAAAAAA… NC_000001.11:16416680:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(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 rs71574184

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

rs71574184