Name: rs71139633
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.

rs71139633

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:4461557-4461568 (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: delCCC / delCC / delC / dupC / dup…
delCCC / delCC / delC / dupC / dupCC / dupCCC / dup(C)₅ / dup(C)₆ / dup(C)₇ / dup(C)₈ / dup(C)₉ / dup(C)₁₀ / dup(C)₁₁ / ins(C)₁₃ / ins(C)₁₄
Variation Type: Indel Insertion and Deletion
Frequency: delC=0.03197 (361/11292, ALFA)
(C)₁₂=0.3988 (1997/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NMRAL1 : 500B Downstream 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	11292	CCCCCCCCCCCC=0.96334	CCCCCCCCC=0.00000, CCCCCCCCCC=0.00000, CCCCCCCCCCC=0.03197, CCCCCCCCCCCCC=0.00443, CCCCCCCCCCCCCC=0.00027, CCCCCCCCCCCCCCC=0.00000	0.940452	0.004706	0.054842	32
European	Sub	9276	CCCCCCCCCCCC=0.9554	CCCCCCCCC=0.0000, CCCCCCCCCC=0.0000, CCCCCCCCCCC=0.0389, CCCCCCCCCCCCC=0.0054, CCCCCCCCCCCCCC=0.0003, CCCCCCCCCCCCCCC=0.0000	0.927164	0.005756	0.06708	30
African	Sub	1182	CCCCCCCCCCCC=1.0000	CCCCCCCCC=0.0000, CCCCCCCCCC=0.0000, CCCCCCCCCCC=0.0000, CCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCCC=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	42	CCCCCCCCCCCC=1.00	CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
African American	Sub	1140	CCCCCCCCCCCC=1.0000	CCCCCCCCC=0.0000, CCCCCCCCCC=0.0000, CCCCCCCCCCC=0.0000, CCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCCC=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	62	CCCCCCCCCCCC=1.00	CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	52	CCCCCCCCCCCC=1.00	CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	10	CCCCCCCCCCCC=1.0	CCCCCCCCC=0.0, CCCCCCCCCC=0.0, CCCCCCCCCCC=0.0, CCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCCC=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	82	CCCCCCCCCCCC=1.00	CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	340	CCCCCCCCCCCC=1.000	CCCCCCCCC=0.000, CCCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCCC=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	64	CCCCCCCCCCCC=1.00	CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Other	Sub	286	CCCCCCCCCCCC=1.000	CCCCCCCCC=0.000, CCCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCCC=0.000	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
Allele Frequency Aggregator	Total	Global	11292	(C)₁₂=0.96334	delCCC=0.00000, delCC=0.00000, delC=0.03197, dupC=0.00443, dupCC=0.00027, dupCCC=0.00000
Allele Frequency Aggregator	European	Sub	9276	(C)₁₂=0.9554	delCCC=0.0000, delCC=0.0000, delC=0.0389, dupC=0.0054, dupCC=0.0003, dupCCC=0.0000
Allele Frequency Aggregator	African	Sub	1182	(C)₁₂=1.0000	delCCC=0.0000, delCC=0.0000, delC=0.0000, dupC=0.0000, dupCC=0.0000, dupCCC=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	340	(C)₁₂=1.000	delCCC=0.000, delCC=0.000, delC=0.000, dupC=0.000, dupCC=0.000, dupCCC=0.000
Allele Frequency Aggregator	Other	Sub	286	(C)₁₂=1.000	delCCC=0.000, delCC=0.000, delC=0.000, dupC=0.000, dupCC=0.000, dupCCC=0.000
Allele Frequency Aggregator	Latin American 1	Sub	82	(C)₁₂=1.00	delCCC=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00
Allele Frequency Aggregator	South Asian	Sub	64	(C)₁₂=1.00	delCCC=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00
Allele Frequency Aggregator	Asian	Sub	62	(C)₁₂=1.00	delCCC=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00
1000Genomes	Global	Study-wide	5008	(C)₁₂=0.3988	delC=0.6012
1000Genomes	African	Sub	1322	(C)₁₂=0.4138	delC=0.5862
1000Genomes	East Asian	Sub	1008	(C)₁₂=0.3036	delC=0.6964
1000Genomes	Europe	Sub	1006	(C)₁₂=0.4642	delC=0.5358
1000Genomes	South Asian	Sub	978	(C)₁₂=0.418	delC=0.582
1000Genomes	American	Sub	694	(C)₁₂=0.386	delC=0.614

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 16	NC_000016.10:g.4461566_4461568del
GRCh38.p14 chr 16	NC_000016.10:g.4461567_4461568del
GRCh38.p14 chr 16	NC_000016.10:g.4461568del
GRCh38.p14 chr 16	NC_000016.10:g.4461568dup
GRCh38.p14 chr 16	NC_000016.10:g.4461567_4461568dup
GRCh38.p14 chr 16	NC_000016.10:g.4461566_4461568dup
GRCh38.p14 chr 16	NC_000016.10:g.4461564_4461568dup
GRCh38.p14 chr 16	NC_000016.10:g.4461563_4461568dup
GRCh38.p14 chr 16	NC_000016.10:g.4461562_4461568dup
GRCh38.p14 chr 16	NC_000016.10:g.4461561_4461568dup
GRCh38.p14 chr 16	NC_000016.10:g.4461560_4461568dup
GRCh38.p14 chr 16	NC_000016.10:g.4461559_4461568dup
GRCh38.p14 chr 16	NC_000016.10:g.4461558_4461568dup
GRCh38.p14 chr 16	NC_000016.10:g.4461568_4461569insCCCCCCCCCCCCC
GRCh38.p14 chr 16	NC_000016.10:g.4461568_4461569insCCCCCCCCCCCCCC
GRCh37.p13 chr 16	NC_000016.9:g.4511567_4511569del
GRCh37.p13 chr 16	NC_000016.9:g.4511568_4511569del
GRCh37.p13 chr 16	NC_000016.9:g.4511569del
GRCh37.p13 chr 16	NC_000016.9:g.4511569dup
GRCh37.p13 chr 16	NC_000016.9:g.4511568_4511569dup
GRCh37.p13 chr 16	NC_000016.9:g.4511567_4511569dup
GRCh37.p13 chr 16	NC_000016.9:g.4511565_4511569dup
GRCh37.p13 chr 16	NC_000016.9:g.4511564_4511569dup
GRCh37.p13 chr 16	NC_000016.9:g.4511563_4511569dup
GRCh37.p13 chr 16	NC_000016.9:g.4511562_4511569dup
GRCh37.p13 chr 16	NC_000016.9:g.4511561_4511569dup
GRCh37.p13 chr 16	NC_000016.9:g.4511560_4511569dup
GRCh37.p13 chr 16	NC_000016.9:g.4511559_4511569dup
GRCh37.p13 chr 16	NC_000016.9:g.4511569_4511570insCCCCCCCCCCCCC
GRCh37.p13 chr 16	NC_000016.9:g.4511569_4511570insCCCCCCCCCCCCCC
GRCh38.p14 chr 16 alt locus HSCHR16_3_CTG1	NT_187608.1:g.163889_163891del
GRCh38.p14 chr 16 alt locus HSCHR16_3_CTG1	NT_187608.1:g.163890_163891del
GRCh38.p14 chr 16 alt locus HSCHR16_3_CTG1	NT_187608.1:g.163891del
GRCh38.p14 chr 16 alt locus HSCHR16_3_CTG1	NT_187608.1:g.163891dup
GRCh38.p14 chr 16 alt locus HSCHR16_3_CTG1	NT_187608.1:g.163890_163891dup
GRCh38.p14 chr 16 alt locus HSCHR16_3_CTG1	NT_187608.1:g.163889_163891dup
GRCh38.p14 chr 16 alt locus HSCHR16_3_CTG1	NT_187608.1:g.163887_163891dup
GRCh38.p14 chr 16 alt locus HSCHR16_3_CTG1	NT_187608.1:g.163886_163891dup
GRCh38.p14 chr 16 alt locus HSCHR16_3_CTG1	NT_187608.1:g.163885_163891dup
GRCh38.p14 chr 16 alt locus HSCHR16_3_CTG1	NT_187608.1:g.163884_163891dup
GRCh38.p14 chr 16 alt locus HSCHR16_3_CTG1	NT_187608.1:g.163883_163891dup
GRCh38.p14 chr 16 alt locus HSCHR16_3_CTG1	NT_187608.1:g.163882_163891dup
GRCh38.p14 chr 16 alt locus HSCHR16_3_CTG1	NT_187608.1:g.163881_163891dup
GRCh38.p14 chr 16 alt locus HSCHR16_3_CTG1	NT_187608.1:g.163891_163892insCCCCCCCCCCCCC
GRCh38.p14 chr 16 alt locus HSCHR16_3_CTG1	NT_187608.1:g.163891_163892insCCCCCCCCCCCCCC

Gene: NMRAL1, NmrA like redox sensor 1 (minus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
NMRAL1 transcript variant 2	NM_001305141.3:c.	N/A	Downstream Transcript Variant
NMRAL1 transcript variant 3	NM_001305142.3:c.	N/A	Downstream Transcript Variant
NMRAL1 transcript variant 4	NM_001351994.2:c.	N/A	Downstream Transcript Variant
NMRAL1 transcript variant 5	NM_001351995.2:c.	N/A	Downstream Transcript Variant
NMRAL1 transcript variant 6	NM_001351996.2:c.	N/A	Downstream Transcript Variant
NMRAL1 transcript variant 1	NM_020677.6:c.	N/A	Downstream Transcript Variant
NMRAL1 transcript variant 7	NR_147845.2:n.	N/A	Downstream Transcript Variant
NMRAL1 transcript variant X1	XM_047434381.1:c.	N/A	Downstream Transcript Variant
NMRAL1 transcript variant X2	XM_047434382.1:c.	N/A	Downstream Transcript Variant
NMRAL1 transcript variant X7	XM_047434385.1:c.	N/A	Downstream Transcript Variant
NMRAL1 transcript variant X8	XM_047434386.1:c.	N/A	Downstream Transcript Variant
NMRAL1 transcript variant X9	XM_047434387.1:c.	N/A	Downstream Transcript Variant
NMRAL1 transcript variant X3	XM_017023486.3:c.	N/A	N/A
NMRAL1 transcript variant X6	XM_017023488.3:c.	N/A	N/A
NMRAL1 transcript variant X4	XM_047434383.1:c.	N/A	N/A
NMRAL1 transcript variant X5	XM_047434384.1:c.	N/A	N/A

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	(C)₁₂=	delCCC	delCC	delC	dupC	dupCC	dupCCC	dup(C)₅	dup(C)₆	dup(C)₇	dup(C)₈	dup(C)₉	dup(C)₁₀	dup(C)₁₁	ins(C)₁₃	ins(C)₁₄
GRCh38.p14 chr 16	NC_000016.10:g.4461557_4461568=	NC_000016.10:g.4461566_4461568del	NC_000016.10:g.4461567_4461568del	NC_000016.10:g.4461568del	NC_000016.10:g.4461568dup	NC_000016.10:g.4461567_4461568dup	NC_000016.10:g.4461566_4461568dup	NC_000016.10:g.4461564_4461568dup	NC_000016.10:g.4461563_4461568dup	NC_000016.10:g.4461562_4461568dup	NC_000016.10:g.4461561_4461568dup	NC_000016.10:g.4461560_4461568dup	NC_000016.10:g.4461559_4461568dup	NC_000016.10:g.4461558_4461568dup	NC_000016.10:g.4461568_4461569insCCCCCCCCCCCCC	NC_000016.10:g.4461568_4461569insCCCCCCCCCCCCCC
GRCh37.p13 chr 16	NC_000016.9:g.4511558_4511569=	NC_000016.9:g.4511567_4511569del	NC_000016.9:g.4511568_4511569del	NC_000016.9:g.4511569del	NC_000016.9:g.4511569dup	NC_000016.9:g.4511568_4511569dup	NC_000016.9:g.4511567_4511569dup	NC_000016.9:g.4511565_4511569dup	NC_000016.9:g.4511564_4511569dup	NC_000016.9:g.4511563_4511569dup	NC_000016.9:g.4511562_4511569dup	NC_000016.9:g.4511561_4511569dup	NC_000016.9:g.4511560_4511569dup	NC_000016.9:g.4511559_4511569dup	NC_000016.9:g.4511569_4511570insCCCCCCCCCCCCC	NC_000016.9:g.4511569_4511570insCCCCCCCCCCCCCC
GRCh38.p14 chr 16 alt locus HSCHR16_3_CTG1	NT_187608.1:g.163880_163891=	NT_187608.1:g.163889_163891del	NT_187608.1:g.163890_163891del	NT_187608.1:g.163891del	NT_187608.1:g.163891dup	NT_187608.1:g.163890_163891dup	NT_187608.1:g.163889_163891dup	NT_187608.1:g.163887_163891dup	NT_187608.1:g.163886_163891dup	NT_187608.1:g.163885_163891dup	NT_187608.1:g.163884_163891dup	NT_187608.1:g.163883_163891dup	NT_187608.1:g.163882_163891dup	NT_187608.1:g.163881_163891dup	NT_187608.1:g.163891_163892insCCCCCCCCCCCCC	NT_187608.1:g.163891_163892insCCCCCCCCCCCCCC

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#.

46 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss83582698	Oct 12, 2018 (152)
2	HUMANGENOME_JCVI	ss95670225	Dec 05, 2013 (138)
3	HUMANGENOME_JCVI	ss96709636	Feb 13, 2009 (137)
4	PJP	ss294878257	May 09, 2011 (134)
5	SSMP	ss664314077	Apr 01, 2015 (144)
6	1000GENOMES	ss1375489008	Aug 21, 2014 (142)
7	BEROUKHIMLAB	ss3644395818	Oct 12, 2018 (152)
8	EVA_DECODE	ss3698712365	Jul 13, 2019 (153)
9	EVA_DECODE	ss3698712366	Jul 13, 2019 (153)
10	EVA_DECODE	ss3698712367	Jul 13, 2019 (153)
11	EVA_DECODE	ss3698712368	Jul 13, 2019 (153)
12	PACBIO	ss3787962457	Jul 13, 2019 (153)
13	PACBIO	ss3792957234	Jul 13, 2019 (153)
14	PACBIO	ss3797842122	Jul 13, 2019 (153)
15	KHV_HUMAN_GENOMES	ss3818901864	Jul 13, 2019 (153)
16	EVA	ss3834440537	Apr 27, 2020 (154)
17	GNOMAD	ss4295868696	Apr 27, 2021 (155)
18	GNOMAD	ss4295868697	Apr 27, 2021 (155)
19	GNOMAD	ss4295868698	Apr 27, 2021 (155)
20	GNOMAD	ss4295868699	Apr 27, 2021 (155)
21	GNOMAD	ss4295868700	Apr 27, 2021 (155)
22	GNOMAD	ss4295868701	Apr 27, 2021 (155)
23	GNOMAD	ss4295868702	Apr 27, 2021 (155)
24	GNOMAD	ss4295868703	Apr 27, 2021 (155)
25	GNOMAD	ss4295868704	Apr 27, 2021 (155)
26	GNOMAD	ss4295868705	Apr 27, 2021 (155)
27	GNOMAD	ss4295868706	Apr 27, 2021 (155)
28	GNOMAD	ss4295868707	Apr 27, 2021 (155)
29	GNOMAD	ss4295868709	Apr 27, 2021 (155)
30	GNOMAD	ss4295868710	Apr 27, 2021 (155)
31	GNOMAD	ss4295868711	Apr 27, 2021 (155)
32	TOMMO_GENOMICS	ss5218134871	Apr 27, 2021 (155)
33	TOMMO_GENOMICS	ss5218134872	Apr 27, 2021 (155)
34	TOMMO_GENOMICS	ss5218134873	Apr 27, 2021 (155)
35	TOMMO_GENOMICS	ss5218134874	Apr 27, 2021 (155)
36	1000G_HIGH_COVERAGE	ss5299907116	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5493457275	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5493457277	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5493457278	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5493457279	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5493457280	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5772531099	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5772531100	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5772531101	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5772531103	Oct 16, 2022 (156)
46	EVA	ss5851462546	Oct 16, 2022 (156)
47	1000Genomes	NC_000016.9 - 4511558	Oct 12, 2018 (152)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 481023793 (NC_000016.10:4461556::C 3742/70518) Row 481023794 (NC_000016.10:4461556::CC 275/70564) Row 481023795 (NC_000016.10:4461556::CCC 5/70584)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 481023793 (NC_000016.10:4461556::C 3742/70518) Row 481023794 (NC_000016.10:4461556::CC 275/70564) Row 481023795 (NC_000016.10:4461556::CCC 5/70584)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 481023793 (NC_000016.10:4461556::C 3742/70518) Row 481023794 (NC_000016.10:4461556::CC 275/70564) Row 481023795 (NC_000016.10:4461556::CCC 5/70584)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 481023793 (NC_000016.10:4461556::C 3742/70518) Row 481023794 (NC_000016.10:4461556::CC 275/70564) Row 481023795 (NC_000016.10:4461556::CCC 5/70584)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 481023793 (NC_000016.10:4461556::C 3742/70518) Row 481023794 (NC_000016.10:4461556::CC 275/70564) Row 481023795 (NC_000016.10:4461556::CCC 5/70584)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 481023793 (NC_000016.10:4461556::C 3742/70518) Row 481023794 (NC_000016.10:4461556::CC 275/70564) Row 481023795 (NC_000016.10:4461556::CCC 5/70584)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 481023793 (NC_000016.10:4461556::C 3742/70518) Row 481023794 (NC_000016.10:4461556::CC 275/70564) Row 481023795 (NC_000016.10:4461556::CCC 5/70584)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 481023793 (NC_000016.10:4461556::C 3742/70518) Row 481023794 (NC_000016.10:4461556::CC 275/70564) Row 481023795 (NC_000016.10:4461556::CCC 5/70584)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 481023793 (NC_000016.10:4461556::C 3742/70518) Row 481023794 (NC_000016.10:4461556::CC 275/70564) Row 481023795 (NC_000016.10:4461556::CCC 5/70584)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 481023793 (NC_000016.10:4461556::C 3742/70518) Row 481023794 (NC_000016.10:4461556::CC 275/70564) Row 481023795 (NC_000016.10:4461556::CCC 5/70584)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 481023793 (NC_000016.10:4461556::C 3742/70518) Row 481023794 (NC_000016.10:4461556::CC 275/70564) Row 481023795 (NC_000016.10:4461556::CCC 5/70584)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 481023793 (NC_000016.10:4461556::C 3742/70518) Row 481023794 (NC_000016.10:4461556::CC 275/70564) Row 481023795 (NC_000016.10:4461556::CCC 5/70584)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 481023793 (NC_000016.10:4461556::C 3742/70518) Row 481023794 (NC_000016.10:4461556::CC 275/70564) Row 481023795 (NC_000016.10:4461556::CCC 5/70584)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 481023793 (NC_000016.10:4461556::C 3742/70518) Row 481023794 (NC_000016.10:4461556::CC 275/70564) Row 481023795 (NC_000016.10:4461556::CCC 5/70584)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 481023793 (NC_000016.10:4461556::C 3742/70518) Row 481023794 (NC_000016.10:4461556::CC 275/70564) Row 481023795 (NC_000016.10:4461556::CCC 5/70584)...	-	Apr 27, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 76104178 (NC_000016.9:4511557:C: 1014/15570) Row 76104179 (NC_000016.9:4511557:CC: 21/15570) Row 76104180 (NC_000016.9:4511557::C 2129/15570)...	-	Apr 27, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 76104178 (NC_000016.9:4511557:C: 1014/15570) Row 76104179 (NC_000016.9:4511557:CC: 21/15570) Row 76104180 (NC_000016.9:4511557::C 2129/15570)...	-	Apr 27, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 76104178 (NC_000016.9:4511557:C: 1014/15570) Row 76104179 (NC_000016.9:4511557:CC: 21/15570) Row 76104180 (NC_000016.9:4511557::C 2129/15570)...	-	Apr 27, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 76104178 (NC_000016.9:4511557:C: 1014/15570) Row 76104179 (NC_000016.9:4511557:CC: 21/15570) Row 76104180 (NC_000016.9:4511557::C 2129/15570)...	-	Apr 27, 2021 (155)
67	14KJPN Submission ignored due to conflicting rows: Row 106368203 (NC_000016.10:4461556:C: 2223/27792) Row 106368204 (NC_000016.10:4461556::C 5363/27792) Row 106368205 (NC_000016.10:4461556:CC: 44/27792)...	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 106368203 (NC_000016.10:4461556:C: 2223/27792) Row 106368204 (NC_000016.10:4461556::C 5363/27792) Row 106368205 (NC_000016.10:4461556:CC: 44/27792)...	-	Oct 16, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 106368203 (NC_000016.10:4461556:C: 2223/27792) Row 106368204 (NC_000016.10:4461556::C 5363/27792) Row 106368205 (NC_000016.10:4461556:CC: 44/27792)...	-	Oct 16, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 106368203 (NC_000016.10:4461556:C: 2223/27792) Row 106368204 (NC_000016.10:4461556::C 5363/27792) Row 106368205 (NC_000016.10:4461556:CC: 44/27792)...	-	Oct 16, 2022 (156)
71	ALFA	NC_000016.10 - 4461557	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)
rs71402538	May 11, 2012 (137)
rs376645898	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4295868711	NC_000016.10:4461556:CCC:	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCC	(self)
15745274192	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCC	(self)
ss3834440537, ss5218134872	NC_000016.9:4511557:CC:	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCC	(self)
ss3698712368, ss4295868710, ss5493457279, ss5772531101	NC_000016.10:4461556:CC:	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCC	(self)
15745274192	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCC	(self)
ss294878257	NC_000016.8:4451569:C:	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
68248922, ss664314077, ss1375489008, ss3644395818, ss3787962457, ss3792957234, ss3797842122, ss5218134871	NC_000016.9:4511557:C:	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
ss3818901864, ss4295868709, ss5299907116, ss5493457275, ss5772531099, ss5851462546	NC_000016.10:4461556:C:	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
15745274192	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
ss3698712367	NC_000016.10:4461557:C:	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
ss96709636	NT_010393.16:4451557:C:	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
ss95670225	NT_010393.16:4451568:C:	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
ss5218134873	NC_000016.9:4511557::C	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss4295868696, ss5493457278, ss5772531100	NC_000016.10:4461556::C	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
15745274192	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss3698712366	NC_000016.10:4461558::C	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss83582698	NT_010393.16:4451569::C	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss5218134874	NC_000016.9:4511557::CC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
ss4295868697, ss5772531103	NC_000016.10:4461556::CC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
15745274192	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCCC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
ss3698712365	NC_000016.10:4461558::CC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
ss4295868698	NC_000016.10:4461556::CCC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCCCC	(self)
15745274192	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCCCC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCCCC	(self)
ss4295868699, ss5493457277	NC_000016.10:4461556::CCCCC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCCCCCC	(self)
ss4295868700, ss5493457280	NC_000016.10:4461556::CCCCCC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCCCCCCC	(self)
ss4295868701	NC_000016.10:4461556::CCCCCCC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCCCCCCCC	(self)
ss4295868702	NC_000016.10:4461556::CCCCCCCC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCCCCCCCCC	(self)
ss4295868703	NC_000016.10:4461556::CCCCCCCCC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCCCCCCCCCC	(self)
ss4295868704	NC_000016.10:4461556::CCCCCCCCCC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCCCCCCCCCCC	(self)
ss4295868705	NC_000016.10:4461556::CCCCCCCCCCC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCCCCCCCCCCCC	(self)
ss4295868706	NC_000016.10:4461556::CCCCCCCCCCCCC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCCCCCCCCCCCCCC	(self)
ss4295868707	NC_000016.10:4461556::CCCCCCCCCCCC… NC_000016.10:4461556::CCCCCCCCCCCCCC	NC_000016.10:4461556:CCCCCCCCCCCC:… NC_000016.10:4461556:CCCCCCCCCCCC:CCCCCCCCCCCCCCCCCCCCCCCCCC	(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 rs71139633

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

rs71139633