Name: rs71029603
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.

rs71029603

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:3022920-3022936 (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
Variation Type: Indel Insertion and Deletion
Frequency: delAAA=0.05848 (826/14124, ALFA)
delAAA=0.201 (114/566, NorthernSweden)
delAAA=0.47 (19/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CARD11 : 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	14124	AAAAAAAAAAAAAAAAA=0.94053	AAAAAAAAAAAAA=0.00057, AAAAAAAAAAAAAA=0.05848, AAAAAAAAAAAAAAAA=0.00035, AAAAAAAAAAAAAAAAAAA=0.00007, AAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000	0.894647	0.011105	0.094248	32
European	Sub	10480	AAAAAAAAAAAAAAAAA=0.91994	AAAAAAAAAAAAA=0.00076, AAAAAAAAAAAAAA=0.07882, AAAAAAAAAAAAAAAA=0.00038, AAAAAAAAAAAAAAAAAAA=0.00010, AAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000	0.857774	0.014991	0.127234	32
African	Sub	2372	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	88	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	2284	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	102	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
East Asian	Sub	82	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	20	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	126	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	564	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	80	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	400	AAAAAAAAAAAAAAAAA=0.998	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.003, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=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	14124	(A)₁₇=0.94053	del(A)₄=0.00057, delAAA=0.05848, delAA=0.00000, delA=0.00035, dupA=0.00000, dupAA=0.00007
Allele Frequency Aggregator	European	Sub	10480	(A)₁₇=0.91994	del(A)₄=0.00076, delAAA=0.07882, delAA=0.00000, delA=0.00038, dupA=0.00000, dupAA=0.00010
Allele Frequency Aggregator	African	Sub	2372	(A)₁₇=1.0000	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	564	(A)₁₇=1.000	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	400	(A)₁₇=0.998	del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.003, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	126	(A)₁₇=1.000	del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Asian	Sub	102	(A)₁₇=1.000	del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	South Asian	Sub	80	(A)₁₇=1.00	del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Northern Sweden	ACPOP	Study-wide	566	(A)₁₇=0.799	delAAA=0.201
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₇=0.53	delAAA=0.47

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.3022932_3022936del
GRCh38.p14 chr 7	NC_000007.14:g.3022933_3022936del
GRCh38.p14 chr 7	NC_000007.14:g.3022934_3022936del
GRCh38.p14 chr 7	NC_000007.14:g.3022935_3022936del
GRCh38.p14 chr 7	NC_000007.14:g.3022936del
GRCh38.p14 chr 7	NC_000007.14:g.3022936dup
GRCh38.p14 chr 7	NC_000007.14:g.3022935_3022936dup
GRCh37.p13 chr 7	NC_000007.13:g.3062566_3062570del
GRCh37.p13 chr 7	NC_000007.13:g.3062567_3062570del
GRCh37.p13 chr 7	NC_000007.13:g.3062568_3062570del
GRCh37.p13 chr 7	NC_000007.13:g.3062569_3062570del
GRCh37.p13 chr 7	NC_000007.13:g.3062570del
GRCh37.p13 chr 7	NC_000007.13:g.3062570dup
GRCh37.p13 chr 7	NC_000007.13:g.3062569_3062570dup
CARD11 RefSeqGene (LRG_729)	NG_027759.1:g.25952_25956del
CARD11 RefSeqGene (LRG_729)	NG_027759.1:g.25953_25956del
CARD11 RefSeqGene (LRG_729)	NG_027759.1:g.25954_25956del
CARD11 RefSeqGene (LRG_729)	NG_027759.1:g.25955_25956del
CARD11 RefSeqGene (LRG_729)	NG_027759.1:g.25956del
CARD11 RefSeqGene (LRG_729)	NG_027759.1:g.25956dup
CARD11 RefSeqGene (LRG_729)	NG_027759.1:g.25955_25956dup

Gene: CARD11, caspase recruitment domain family member 11 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CARD11 transcript variant 1	NM_001324281.3:c.-187+207… NM_001324281.3:c.-187+20743_-187+20747del	N/A	Intron Variant
CARD11 transcript variant 2	NM_032415.7:c.-126+20743_… NM_032415.7:c.-126+20743_-126+20747del	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)₁₇=	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA
GRCh38.p14 chr 7	NC_000007.14:g.3022920_3022936=	NC_000007.14:g.3022932_3022936del	NC_000007.14:g.3022933_3022936del	NC_000007.14:g.3022934_3022936del	NC_000007.14:g.3022935_3022936del	NC_000007.14:g.3022936del	NC_000007.14:g.3022936dup	NC_000007.14:g.3022935_3022936dup
GRCh37.p13 chr 7	NC_000007.13:g.3062554_3062570=	NC_000007.13:g.3062566_3062570del	NC_000007.13:g.3062567_3062570del	NC_000007.13:g.3062568_3062570del	NC_000007.13:g.3062569_3062570del	NC_000007.13:g.3062570del	NC_000007.13:g.3062570dup	NC_000007.13:g.3062569_3062570dup
CARD11 RefSeqGene (LRG_729)	NG_027759.1:g.25940_25956=	NG_027759.1:g.25952_25956del	NG_027759.1:g.25953_25956del	NG_027759.1:g.25954_25956del	NG_027759.1:g.25955_25956del	NG_027759.1:g.25956del	NG_027759.1:g.25956dup	NG_027759.1:g.25955_25956dup
CARD11 transcript variant 1	NM_001324281.3:c.-187+20747=	NM_001324281.3:c.-187+20743_-187+20747del	NM_001324281.3:c.-187+20744_-187+20747del	NM_001324281.3:c.-187+20745_-187+20747del	NM_001324281.3:c.-187+20746_-187+20747del	NM_001324281.3:c.-187+20747del	NM_001324281.3:c.-187+20747dup	NM_001324281.3:c.-187+20746_-187+20747dup
CARD11 transcript	NM_032415.4:c.-126+20747=	NM_032415.4:c.-126+20743_-126+20747del	NM_032415.4:c.-126+20744_-126+20747del	NM_032415.4:c.-126+20745_-126+20747del	NM_032415.4:c.-126+20746_-126+20747del	NM_032415.4:c.-126+20747del	NM_032415.4:c.-126+20747dup	NM_032415.4:c.-126+20746_-126+20747dup
CARD11 transcript variant 2	NM_032415.7:c.-126+20747=	NM_032415.7:c.-126+20743_-126+20747del	NM_032415.7:c.-126+20744_-126+20747del	NM_032415.7:c.-126+20745_-126+20747del	NM_032415.7:c.-126+20746_-126+20747del	NM_032415.7:c.-126+20747del	NM_032415.7:c.-126+20747dup	NM_032415.7:c.-126+20746_-126+20747dup
CARD11 transcript variant X2	XM_005249891.1:c.-191+20747=	XM_005249891.1:c.-191+20743_-191+20747del	XM_005249891.1:c.-191+20744_-191+20747del	XM_005249891.1:c.-191+20745_-191+20747del	XM_005249891.1:c.-191+20746_-191+20747del	XM_005249891.1:c.-191+20747del	XM_005249891.1:c.-191+20747dup	XM_005249891.1:c.-191+20746_-191+20747dup
CARD11 transcript variant X3	XM_005249892.1:c.-126+20747=	XM_005249892.1:c.-126+20743_-126+20747del	XM_005249892.1:c.-126+20744_-126+20747del	XM_005249892.1:c.-126+20745_-126+20747del	XM_005249892.1:c.-126+20746_-126+20747del	XM_005249892.1:c.-126+20747del	XM_005249892.1:c.-126+20747dup	XM_005249892.1:c.-126+20746_-126+20747dup
CARD11 transcript variant X4	XM_005249893.1:c.-126+20747=	XM_005249893.1:c.-126+20743_-126+20747del	XM_005249893.1:c.-126+20744_-126+20747del	XM_005249893.1:c.-126+20745_-126+20747del	XM_005249893.1:c.-126+20746_-126+20747del	XM_005249893.1:c.-126+20747del	XM_005249893.1:c.-126+20747dup	XM_005249893.1:c.-126+20746_-126+20747dup

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#.

42 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95450555	Feb 13, 2009 (130)
2	EVA_GENOME_DK	ss1576926544	Apr 01, 2015 (144)
3	SWEGEN	ss3000486707	Nov 08, 2017 (151)
4	EVA_DECODE	ss3718935162	Jul 13, 2019 (153)
5	EVA_DECODE	ss3718935163	Jul 13, 2019 (153)
6	EVA_DECODE	ss3718935164	Jul 13, 2019 (153)
7	EVA_DECODE	ss3718935165	Jul 13, 2019 (153)
8	EVA_DECODE	ss3718935166	Jul 13, 2019 (153)
9	EVA_DECODE	ss3718935167	Jul 13, 2019 (153)
10	ACPOP	ss3734279908	Jul 13, 2019 (153)
11	PACBIO	ss3791026954	Jul 13, 2019 (153)
12	PACBIO	ss3795906622	Jul 13, 2019 (153)
13	EVA	ss3830366385	Apr 26, 2020 (154)
14	KOGIC	ss3960724409	Apr 26, 2020 (154)
15	KOGIC	ss3960724410	Apr 26, 2020 (154)
16	KOGIC	ss3960724411	Apr 26, 2020 (154)
17	KOGIC	ss3960724412	Apr 26, 2020 (154)
18	GNOMAD	ss4156974937	Apr 26, 2021 (155)
19	GNOMAD	ss4156974938	Apr 26, 2021 (155)
20	GNOMAD	ss4156974939	Apr 26, 2021 (155)
21	GNOMAD	ss4156974940	Apr 26, 2021 (155)
22	GNOMAD	ss4156974941	Apr 26, 2021 (155)
23	GNOMAD	ss4156974942	Apr 26, 2021 (155)
24	GNOMAD	ss4156974943	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5181434527	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5181434528	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5181434529	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5181434530	Apr 26, 2021 (155)
29	1000G_HIGH_COVERAGE	ss5271523858	Oct 13, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5271523859	Oct 13, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5271523861	Oct 13, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5271523862	Oct 13, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5271523863	Oct 13, 2022 (156)
34	HUGCELL_USP	ss5468846317	Oct 13, 2022 (156)
35	HUGCELL_USP	ss5468846318	Oct 13, 2022 (156)
36	HUGCELL_USP	ss5468846319	Oct 13, 2022 (156)
37	HUGCELL_USP	ss5468846321	Oct 13, 2022 (156)
38	TOMMO_GENOMICS	ss5720778346	Oct 13, 2022 (156)
39	TOMMO_GENOMICS	ss5720778347	Oct 13, 2022 (156)
40	TOMMO_GENOMICS	ss5720778348	Oct 13, 2022 (156)
41	TOMMO_GENOMICS	ss5720778350	Oct 13, 2022 (156)
42	EVA	ss5855725479	Oct 13, 2022 (156)
43	The Danish reference pan genome	NC_000007.13 - 3062554	Apr 26, 2020 (154)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 250493896 (NC_000007.14:3022919::A 69/81156) Row 250493897 (NC_000007.14:3022919::AA 29/81166) Row 250493898 (NC_000007.14:3022919:A: 3381/81160)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 250493896 (NC_000007.14:3022919::A 69/81156) Row 250493897 (NC_000007.14:3022919::AA 29/81166) Row 250493898 (NC_000007.14:3022919:A: 3381/81160)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 250493896 (NC_000007.14:3022919::A 69/81156) Row 250493897 (NC_000007.14:3022919::AA 29/81166) Row 250493898 (NC_000007.14:3022919:A: 3381/81160)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 250493896 (NC_000007.14:3022919::A 69/81156) Row 250493897 (NC_000007.14:3022919::AA 29/81166) Row 250493898 (NC_000007.14:3022919:A: 3381/81160)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 250493896 (NC_000007.14:3022919::A 69/81156) Row 250493897 (NC_000007.14:3022919::AA 29/81166) Row 250493898 (NC_000007.14:3022919:A: 3381/81160)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 250493896 (NC_000007.14:3022919::A 69/81156) Row 250493897 (NC_000007.14:3022919::AA 29/81166) Row 250493898 (NC_000007.14:3022919:A: 3381/81160)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 250493896 (NC_000007.14:3022919::A 69/81156) Row 250493897 (NC_000007.14:3022919::AA 29/81166) Row 250493898 (NC_000007.14:3022919:A: 3381/81160)...	-	Apr 26, 2021 (155)
51	Korean Genome Project Submission ignored due to conflicting rows: Row 17102410 (NC_000007.14:3022923::A 39/1802) Row 17102411 (NC_000007.14:3022922:A: 87/1802) Row 17102412 (NC_000007.14:3022920:AAA: 136/1802)...	-	Apr 26, 2020 (154)
52	Korean Genome Project Submission ignored due to conflicting rows: Row 17102410 (NC_000007.14:3022923::A 39/1802) Row 17102411 (NC_000007.14:3022922:A: 87/1802) Row 17102412 (NC_000007.14:3022920:AAA: 136/1802)...	-	Apr 26, 2020 (154)
53	Korean Genome Project Submission ignored due to conflicting rows: Row 17102410 (NC_000007.14:3022923::A 39/1802) Row 17102411 (NC_000007.14:3022922:A: 87/1802) Row 17102412 (NC_000007.14:3022920:AAA: 136/1802)...	-	Apr 26, 2020 (154)
54	Korean Genome Project Submission ignored due to conflicting rows: Row 17102410 (NC_000007.14:3022923::A 39/1802) Row 17102411 (NC_000007.14:3022922:A: 87/1802) Row 17102412 (NC_000007.14:3022920:AAA: 136/1802)...	-	Apr 26, 2020 (154)
55	Northern Sweden	NC_000007.13 - 3062554	Jul 13, 2019 (153)
56	8.3KJPN Submission ignored due to conflicting rows: Row 39403834 (NC_000007.13:3062553:AAA: 1343/16754) Row 39403835 (NC_000007.13:3062553:A: 107/16754) Row 39403836 (NC_000007.13:3062553::A 19/16754)...	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 39403834 (NC_000007.13:3062553:AAA: 1343/16754) Row 39403835 (NC_000007.13:3062553:A: 107/16754) Row 39403836 (NC_000007.13:3062553::A 19/16754)...	-	Apr 26, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 39403834 (NC_000007.13:3062553:AAA: 1343/16754) Row 39403835 (NC_000007.13:3062553:A: 107/16754) Row 39403836 (NC_000007.13:3062553::A 19/16754)...	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 39403834 (NC_000007.13:3062553:AAA: 1343/16754) Row 39403835 (NC_000007.13:3062553:A: 107/16754) Row 39403836 (NC_000007.13:3062553::A 19/16754)...	-	Apr 26, 2021 (155)
60	14KJPN Submission ignored due to conflicting rows: Row 54615450 (NC_000007.14:3022919:AAA: 2304/28256) Row 54615451 (NC_000007.14:3022919:A: 163/28256) Row 54615452 (NC_000007.14:3022919::A 38/28256)...	-	Oct 13, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 54615450 (NC_000007.14:3022919:AAA: 2304/28256) Row 54615451 (NC_000007.14:3022919:A: 163/28256) Row 54615452 (NC_000007.14:3022919::A 38/28256)...	-	Oct 13, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 54615450 (NC_000007.14:3022919:AAA: 2304/28256) Row 54615451 (NC_000007.14:3022919:A: 163/28256) Row 54615452 (NC_000007.14:3022919::A 38/28256)...	-	Oct 13, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 54615450 (NC_000007.14:3022919:AAA: 2304/28256) Row 54615451 (NC_000007.14:3022919:A: 163/28256) Row 54615452 (NC_000007.14:3022919::A 38/28256)...	-	Oct 13, 2022 (156)
64	ALFA	NC_000007.14 - 3022920	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
ss4156974943	NC_000007.14:3022919:AAAAA:	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3718935167, ss3960724412, ss4156974942, ss5468846321, ss5720778350	NC_000007.14:3022919:AAAA:	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
666246360	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
1127838, 7564773, ss1576926544, ss3000486707, ss3734279908, ss5181434527	NC_000007.13:3062553:AAA:	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4156974941, ss5271523858, ss5468846317, ss5720778346, ss5855725479	NC_000007.14:3022919:AAA:	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
666246360	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3718935166, ss3960724411	NC_000007.14:3022920:AAA:	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss95450555	NT_007819.17:3052567:AAA:	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5181434530	NC_000007.13:3062553:AA:	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4156974940, ss5271523863	NC_000007.14:3022919:AA:	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
666246360	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3718935165	NC_000007.14:3022921:AA:	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3791026954, ss3795906622, ss5181434528	NC_000007.13:3062553:A:	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4156974939, ss5271523861, ss5468846318, ss5720778347	NC_000007.14:3022919:A:	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
666246360	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3718935164, ss3960724410	NC_000007.14:3022922:A:	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5181434529	NC_000007.13:3062553::A	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4156974937, ss5271523859, ss5468846319, ss5720778348	NC_000007.14:3022919::A	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
666246360	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3718935163, ss3960724409	NC_000007.14:3022923::A	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3830366385	NC_000007.13:3062553::AA	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4156974938, ss5271523862	NC_000007.14:3022919::AA	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
666246360	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3718935162	NC_000007.14:3022923::AA	NC_000007.14:3022919:AAAAAAAAAAAAA… NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(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 rs71029603

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

rs71029603