Name: rs140133886
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.

rs140133886

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:6836800-6836807 (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: delATAT / delAT / dupAT / insATACA…
delATAT / delAT / dupAT / insATACATATGTATAC(AT)₅ / dupATAT / dup(AT)₃ / insATATGCATATG(TA)₃CATATGTATAC(AT)₅ / insATGC(AT)₅ / insATGCATATG(TA)₃CATATGTATACACATGCATATG(TA)₃CATATGTATAC(AT)₅ / insATGCATATG(TA)₃CATATGTATACACATG(TA)₃CATATGTATAC(AT)₅ / insATGCATATG(TA)₃CATATGTATAC(AT)₅ / insATG(TA)₃CATATGTATAC(AT)₅
Variation Type: Indel Insertion and Deletion
Frequency: (AT)₄=0.4201 (2359/5615, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC00707 : 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	5615	ATATATAT=0.4201	ATAT=0.0000, ATATAT=0.0002, ATATATATAT=0.5633, ATATATATATAT=0.0105, ATATATATATGCATATGTATATACATATGTATACATATATATAT=0.0059, ATATATATATACATATGTATACATATATATAT=0.0000, ATATATATATATAT=0.0000, ATATATATATGCATATATATAT=0.0000	0.348491	0.462956	0.188554	32
European	Sub	4515	ATATATAT=0.2806	ATAT=0.0000, ATATAT=0.0002, ATATATATAT=0.6988, ATATATATATAT=0.0131, ATATATATATGCATATGTATATACATATGTATACATATATATAT=0.0073, ATATATATATACATATGTATACATATATATAT=0.0000, ATATATATATATAT=0.0000, ATATATATATGCATATATATAT=0.0000	0.171414	0.588206	0.24038	32
African	Sub	850	ATATATAT=1.000	ATAT=0.000, ATATAT=0.000, ATATATATAT=0.000, ATATATATATAT=0.000, ATATATATATGCATATGTATATACATATGTATACATATATATAT=0.000, ATATATATATACATATGTATACATATATATAT=0.000, ATATATATATATAT=0.000, ATATATATATGCATATATATAT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	38	ATATATAT=1.00	ATAT=0.00, ATATAT=0.00, ATATATATAT=0.00, ATATATATATAT=0.00, ATATATATATGCATATGTATATACATATGTATACATATATATAT=0.00, ATATATATATACATATGTATACATATATATAT=0.00, ATATATATATATAT=0.00, ATATATATATGCATATATATAT=0.00	1.0	0.0	0.0	N/A
African American	Sub	812	ATATATAT=1.000	ATAT=0.000, ATATAT=0.000, ATATATATAT=0.000, ATATATATATAT=0.000, ATATATATATGCATATGTATATACATATGTATACATATATATAT=0.000, ATATATATATACATATGTATACATATATATAT=0.000, ATATATATATATAT=0.000, ATATATATATGCATATATATAT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	44	ATATATAT=1.00	ATAT=0.00, ATATAT=0.00, ATATATATAT=0.00, ATATATATATAT=0.00, ATATATATATGCATATGTATATACATATGTATACATATATATAT=0.00, ATATATATATACATATGTATACATATATATAT=0.00, ATATATATATATAT=0.00, ATATATATATGCATATATATAT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	28	ATATATAT=1.00	ATAT=0.00, ATATAT=0.00, ATATATATAT=0.00, ATATATATATAT=0.00, ATATATATATGCATATGTATATACATATGTATACATATATATAT=0.00, ATATATATATACATATGTATACATATATATAT=0.00, ATATATATATATAT=0.00, ATATATATATGCATATATATAT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	16	ATATATAT=1.00	ATAT=0.00, ATATAT=0.00, ATATATATAT=0.00, ATATATATATAT=0.00, ATATATATATGCATATGTATATACATATGTATACATATATATAT=0.00, ATATATATATACATATGTATACATATATATAT=0.00, ATATATATATATAT=0.00, ATATATATATGCATATATATAT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	16	ATATATAT=1.00	ATAT=0.00, ATATAT=0.00, ATATATATAT=0.00, ATATATATATAT=0.00, ATATATATATGCATATGTATATACATATGTATACATATATATAT=0.00, ATATATATATACATATGTATACATATATATAT=0.00, ATATATATATATAT=0.00, ATATATATATGCATATATATAT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	56	ATATATAT=1.00	ATAT=0.00, ATATAT=0.00, ATATATATAT=0.00, ATATATATATAT=0.00, ATATATATATGCATATGTATATACATATGTATACATATATATAT=0.00, ATATATATATACATATGTATACATATATATAT=0.00, ATATATATATATAT=0.00, ATATATATATGCATATATATAT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	32	ATATATAT=1.00	ATAT=0.00, ATATAT=0.00, ATATATATAT=0.00, ATATATATATAT=0.00, ATATATATATGCATATGTATATACATATGTATACATATATATAT=0.00, ATATATATATACATATGTATACATATATATAT=0.00, ATATATATATATAT=0.00, ATATATATATGCATATATATAT=0.00	1.0	0.0	0.0	N/A
Other	Sub	102	ATATATAT=0.922	ATAT=0.000, ATATAT=0.000, ATATATATAT=0.078, ATATATATATAT=0.000, ATATATATATGCATATGTATATACATATGTATACATATATATAT=0.000, ATATATATATACATATGTATACATATATATAT=0.000, ATATATATATATAT=0.000, ATATATATATGCATATATATAT=0.000	0.921569	0.078431	0.0	27

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	5615	(AT)₄=0.4201	delATAT=0.0000, delAT=0.0002, dupAT=0.5633, insATACATATGTATAC(AT)₅=0.0000, dupATAT=0.0105, dup(AT)₃=0.0000, insATGC(AT)₅=0.0000, insATGCATATG(TA)₃CATATGTATAC(AT)₅=0.0059
Allele Frequency Aggregator	European	Sub	4515	(AT)₄=0.2806	delATAT=0.0000, delAT=0.0002, dupAT=0.6988, insATACATATGTATAC(AT)₅=0.0000, dupATAT=0.0131, dup(AT)₃=0.0000, insATGC(AT)₅=0.0000, insATGCATATG(TA)₃CATATGTATAC(AT)₅=0.0073
Allele Frequency Aggregator	African	Sub	850	(AT)₄=1.000	delATAT=0.000, delAT=0.000, dupAT=0.000, insATACATATGTATAC(AT)₅=0.000, dupATAT=0.000, dup(AT)₃=0.000, insATGC(AT)₅=0.000, insATGCATATG(TA)₃CATATGTATAC(AT)₅=0.000
Allele Frequency Aggregator	Other	Sub	102	(AT)₄=0.922	delATAT=0.000, delAT=0.000, dupAT=0.078, insATACATATGTATAC(AT)₅=0.000, dupATAT=0.000, dup(AT)₃=0.000, insATGC(AT)₅=0.000, insATGCATATG(TA)₃CATATGTATAC(AT)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	56	(AT)₄=1.00	delATAT=0.00, delAT=0.00, dupAT=0.00, insATACATATGTATAC(AT)₅=0.00, dupATAT=0.00, dup(AT)₃=0.00, insATGC(AT)₅=0.00, insATGCATATG(TA)₃CATATGTATAC(AT)₅=0.00
Allele Frequency Aggregator	Asian	Sub	44	(AT)₄=1.00	delATAT=0.00, delAT=0.00, dupAT=0.00, insATACATATGTATAC(AT)₅=0.00, dupATAT=0.00, dup(AT)₃=0.00, insATGC(AT)₅=0.00, insATGCATATG(TA)₃CATATGTATAC(AT)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	32	(AT)₄=1.00	delATAT=0.00, delAT=0.00, dupAT=0.00, insATACATATGTATAC(AT)₅=0.00, dupATAT=0.00, dup(AT)₃=0.00, insATGC(AT)₅=0.00, insATGCATATG(TA)₃CATATGTATAC(AT)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	16	(AT)₄=1.00	delATAT=0.00, delAT=0.00, dupAT=0.00, insATACATATGTATAC(AT)₅=0.00, dupATAT=0.00, dup(AT)₃=0.00, insATGC(AT)₅=0.00, insATGCATATG(TA)₃CATATGTATAC(AT)₅=0.00

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 10	NC_000010.11:g.6836800AT[2]
GRCh38.p14 chr 10	NC_000010.11:g.6836800AT[3]
GRCh38.p14 chr 10	NC_000010.11:g.6836800AT[5]
GRCh38.p14 chr 10	NC_000010.11:g.6836800_6836807AT[5]ACATATGTATACATATATATAT[1]
GRCh38.p14 chr 10	NC_000010.11:g.6836800AT[6]
GRCh38.p14 chr 10	NC_000010.11:g.6836800AT[7]
GRCh38.p14 chr 10	NC_000010.11:g.6836800_6836807AT[6]GCATATGTATATACATATGTATACATATATATAT[1]
GRCh38.p14 chr 10	NC_000010.11:g.6836800_6836807AT[5]GCATATATATAT[1]
GRCh38.p14 chr 10	NC_000010.11:g.6836800_6836807AT[5]GCATATGTATATACATATGTATACACATGCATATGTATATACATATGTATACATATATATAT[1]
GRCh38.p14 chr 10	NC_000010.11:g.6836800_6836807AT[5]GCATATGTATATACATATGTATACACATGTATATACATATGTATACATATATATAT[1]
GRCh38.p14 chr 10	NC_000010.11:g.6836800_6836807AT[5]GCATATGTATATACATATGTATACATATATATAT[1]
GRCh38.p14 chr 10	NC_000010.11:g.6836800_6836807AT[5]GTATATACATATGTATACATATATATAT[1]
GRCh37.p13 chr 10	NC_000010.10:g.6878762AT[2]
GRCh37.p13 chr 10	NC_000010.10:g.6878762AT[3]
GRCh37.p13 chr 10	NC_000010.10:g.6878762AT[5]
GRCh37.p13 chr 10	NC_000010.10:g.6878762_6878769AT[5]ACATATGTATACATATATATAT[1]
GRCh37.p13 chr 10	NC_000010.10:g.6878762AT[6]
GRCh37.p13 chr 10	NC_000010.10:g.6878762AT[7]
GRCh37.p13 chr 10	NC_000010.10:g.6878762_6878769AT[6]GCATATGTATATACATATGTATACATATATATAT[1]
GRCh37.p13 chr 10	NC_000010.10:g.6878762_6878769AT[5]GCATATATATAT[1]
GRCh37.p13 chr 10	NC_000010.10:g.6878762_6878769AT[5]GCATATGTATATACATATGTATACACATGCATATGTATATACATATGTATACATATATATAT[1]
GRCh37.p13 chr 10	NC_000010.10:g.6878762_6878769AT[5]GCATATGTATATACATATGTATACACATGTATATACATATGTATACATATATATAT[1]
GRCh37.p13 chr 10	NC_000010.10:g.6878762_6878769AT[5]GCATATGTATATACATATGTATACATATATATAT[1]
GRCh37.p13 chr 10	NC_000010.10:g.6878762_6878769AT[5]GTATATACATATGTATACATATATATAT[1]

Gene: LINC00707, long intergenic non-protein coding RNA 707 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC00707 transcript	NR_038291.1: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	(AT)₄=	delATAT	delAT	dupAT	insATACATATGTATAC(AT)₅	dupATAT	dup(AT)₃	insATATGCATATG(TA)₃CATATGTATAC(AT)₅	insATGC(AT)₅	insATGCATATG(TA)₃CATATGTATACACATGCATATG(TA)₃CATATGTATAC(AT)₅	insATGCATATG(TA)₃CATATGTATACACATG(TA)₃CATATGTATAC(AT)₅	insATGCATATG(TA)₃CATATGTATAC(AT)₅	insATG(TA)₃CATATGTATAC(AT)₅
GRCh38.p14 chr 10	NC_000010.11:g.6836800_6836807=	NC_000010.11:g.6836800AT[2]	NC_000010.11:g.6836800AT[3]	NC_000010.11:g.6836800AT[5]	NC_000010.11:g.6836800_6836807AT[5]ACATATGTATACATATATATAT[1]	NC_000010.11:g.6836800AT[6]	NC_000010.11:g.6836800AT[7]	NC_000010.11:g.6836800_6836807AT[6]GCATATGTATATACATATGTATACATATATATAT[1]	NC_000010.11:g.6836800_6836807AT[5]GCATATATATAT[1]	NC_000010.11:g.6836800_6836807AT[5]GCATATGTATATACATATGTATACACATGCATATGTATATACATATGTATACATATATATAT[1]	NC_000010.11:g.6836800_6836807AT[5]GCATATGTATATACATATGTATACACATGTATATACATATGTATACATATATATAT[1]	NC_000010.11:g.6836800_6836807AT[5]GCATATGTATATACATATGTATACATATATATAT[1]	NC_000010.11:g.6836800_6836807AT[5]GTATATACATATGTATACATATATATAT[1]
GRCh37.p13 chr 10	NC_000010.10:g.6878762_6878769=	NC_000010.10:g.6878762AT[2]	NC_000010.10:g.6878762AT[3]	NC_000010.10:g.6878762AT[5]	NC_000010.10:g.6878762_6878769AT[5]ACATATGTATACATATATATAT[1]	NC_000010.10:g.6878762AT[6]	NC_000010.10:g.6878762AT[7]	NC_000010.10:g.6878762_6878769AT[6]GCATATGTATATACATATGTATACATATATATAT[1]	NC_000010.10:g.6878762_6878769AT[5]GCATATATATAT[1]	NC_000010.10:g.6878762_6878769AT[5]GCATATGTATATACATATGTATACACATGCATATGTATATACATATGTATACATATATATAT[1]	NC_000010.10:g.6878762_6878769AT[5]GCATATGTATATACATATGTATACACATGTATATACATATGTATACATATATATAT[1]	NC_000010.10:g.6878762_6878769AT[5]GCATATGTATATACATATGTATACATATATATAT[1]	NC_000010.10:g.6878762_6878769AT[5]GTATATACATATGTATACATATATATAT[1]

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#.

45 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GMI	ss287853904	May 09, 2011 (134)
2	GMI	ss288994698	May 04, 2012 (137)
3	LUNTER	ss551996267	Apr 25, 2013 (138)
4	LUNTER	ss552233629	Apr 25, 2013 (138)
5	LUNTER	ss553398865	Apr 25, 2013 (138)
6	SSMP	ss663998220	Apr 01, 2015 (144)
7	DDI	ss1536640946	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1706624262	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1706624264	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1706624266	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1706624269	Apr 01, 2015 (144)
12	JJLAB	ss2030998866	Sep 14, 2016 (149)
13	MCHAISSO	ss3063639234	Nov 08, 2017 (151)
14	MCHAISSO	ss3064458540	Nov 08, 2017 (151)
15	URBANLAB	ss3649281872	Oct 12, 2018 (152)
16	EVA_DECODE	ss3689216267	Jul 13, 2019 (153)
17	EVA_DECODE	ss3689216268	Jul 13, 2019 (153)
18	ACPOP	ss3737031651	Jul 13, 2019 (153)
19	ACPOP	ss3737031653	Jul 13, 2019 (153)
20	ACPOP	ss3737031654	Jul 13, 2019 (153)
21	PACBIO	ss3786571954	Jul 13, 2019 (153)
22	PACBIO	ss3791765693	Jul 13, 2019 (153)
23	PACBIO	ss3796647474	Jul 13, 2019 (153)
24	EVA	ss3839505677	Apr 26, 2020 (154)
25	EVA	ss3844971741	Apr 26, 2020 (154)
26	GNOMAD	ss4212391124	Apr 26, 2021 (155)
27	GNOMAD	ss4212391125	Apr 26, 2021 (155)
28	GNOMAD	ss4212391126	Apr 26, 2021 (155)
29	GNOMAD	ss4212391128	Apr 26, 2021 (155)
30	GNOMAD	ss4212391129	Apr 26, 2021 (155)
31	GNOMAD	ss4212391130	Apr 26, 2021 (155)
32	GNOMAD	ss4212391131	Apr 26, 2021 (155)
33	GNOMAD	ss4212391132	Apr 26, 2021 (155)
34	GNOMAD	ss4212391135	Apr 26, 2021 (155)
35	GNOMAD	ss4212391136	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5196118084	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5196118085	Apr 26, 2021 (155)
38	1000G_HIGH_COVERAGE	ss5282805644	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5478594466	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5478594468	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5478594469	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5740923635	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5740923637	Oct 16, 2022 (156)
44	EVA	ss5849423010	Oct 16, 2022 (156)
45	EVA	ss5877607395	Oct 16, 2022 (156)
46	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 26942604 (NC_000010.10:6878761::AT 2984/3854) Row 26942605 (NC_000010.10:6878761::ATAT 14/3854)	-	Oct 12, 2018 (152)
47	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 26942604 (NC_000010.10:6878761::AT 2984/3854) Row 26942605 (NC_000010.10:6878761::ATAT 14/3854)	-	Oct 12, 2018 (152)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342538747 (NC_000010.11:6836799::AT 83574/131308) Row 342538748 (NC_000010.11:6836799::ATAT 612/131458) Row 342538749 (NC_000010.11:6836799::ATATAT 2/131464)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342538747 (NC_000010.11:6836799::AT 83574/131308) Row 342538748 (NC_000010.11:6836799::ATAT 612/131458) Row 342538749 (NC_000010.11:6836799::ATATAT 2/131464)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342538747 (NC_000010.11:6836799::AT 83574/131308) Row 342538748 (NC_000010.11:6836799::ATAT 612/131458) Row 342538749 (NC_000010.11:6836799::ATATAT 2/131464)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342538747 (NC_000010.11:6836799::AT 83574/131308) Row 342538748 (NC_000010.11:6836799::ATAT 612/131458) Row 342538749 (NC_000010.11:6836799::ATATAT 2/131464)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342538747 (NC_000010.11:6836799::AT 83574/131308) Row 342538748 (NC_000010.11:6836799::ATAT 612/131458) Row 342538749 (NC_000010.11:6836799::ATATAT 2/131464)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342538747 (NC_000010.11:6836799::AT 83574/131308) Row 342538748 (NC_000010.11:6836799::ATAT 612/131458) Row 342538749 (NC_000010.11:6836799::ATATAT 2/131464)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342538747 (NC_000010.11:6836799::AT 83574/131308) Row 342538748 (NC_000010.11:6836799::ATAT 612/131458) Row 342538749 (NC_000010.11:6836799::ATATAT 2/131464)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342538747 (NC_000010.11:6836799::AT 83574/131308) Row 342538748 (NC_000010.11:6836799::ATAT 612/131458) Row 342538749 (NC_000010.11:6836799::ATATAT 2/131464)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342538747 (NC_000010.11:6836799::AT 83574/131308) Row 342538748 (NC_000010.11:6836799::ATAT 612/131458) Row 342538749 (NC_000010.11:6836799::ATATAT 2/131464)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342538747 (NC_000010.11:6836799::AT 83574/131308) Row 342538748 (NC_000010.11:6836799::ATAT 612/131458) Row 342538749 (NC_000010.11:6836799::ATATAT 2/131464)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342538747 (NC_000010.11:6836799::AT 83574/131308) Row 342538748 (NC_000010.11:6836799::ATAT 612/131458) Row 342538749 (NC_000010.11:6836799::ATATAT 2/131464)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342538747 (NC_000010.11:6836799::AT 83574/131308) Row 342538748 (NC_000010.11:6836799::ATAT 612/131458) Row 342538749 (NC_000010.11:6836799::ATATAT 2/131464)...	-	Apr 26, 2021 (155)
60	Northern Sweden Submission ignored due to conflicting rows: Row 10316516 (NC_000010.10:6878761::AT 455/600) Row 10316518 (NC_000010.10:6878761::ATATATATATGCATATGTATATACATATGTATACAT 11/600) Row 10316519 (NC_000010.10:6878761::ATAT 4/600)	-	Jul 13, 2019 (153)
61	Northern Sweden Submission ignored due to conflicting rows: Row 10316516 (NC_000010.10:6878761::AT 455/600) Row 10316518 (NC_000010.10:6878761::ATATATATATGCATATGTATATACATATGTATACAT 11/600) Row 10316519 (NC_000010.10:6878761::ATAT 4/600)	-	Jul 13, 2019 (153)
62	Northern Sweden Submission ignored due to conflicting rows: Row 10316516 (NC_000010.10:6878761::AT 455/600) Row 10316518 (NC_000010.10:6878761::ATATATATATGCATATGTATATACATATGTATACAT 11/600) Row 10316519 (NC_000010.10:6878761::ATAT 4/600)	-	Jul 13, 2019 (153)
63	8.3KJPN Submission ignored due to conflicting rows: Row 54087391 (NC_000010.10:6878761::ATAT 48/13152) Row 54087392 (NC_000010.10:6878761::AT 27/13152)	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 54087391 (NC_000010.10:6878761::ATAT 48/13152) Row 54087392 (NC_000010.10:6878761::AT 27/13152)	-	Apr 26, 2021 (155)
65	14KJPN Submission ignored due to conflicting rows: Row 74760739 (NC_000010.11:6836799::AT 11391/28166) Row 74760741 (NC_000010.11:6836799::ATAT 115/28166)	-	Oct 16, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 74760739 (NC_000010.11:6836799::AT 11391/28166) Row 74760741 (NC_000010.11:6836799::ATAT 115/28166)	-	Oct 16, 2022 (156)
67	UK 10K study - Twins Submission ignored due to conflicting rows: Row 26942604 (NC_000010.10:6878761::AT 2905/3708) Row 26942605 (NC_000010.10:6878761::ATAT 18/3708)	-	Oct 12, 2018 (152)
68	UK 10K study - Twins Submission ignored due to conflicting rows: Row 26942604 (NC_000010.10:6878761::AT 2905/3708) Row 26942605 (NC_000010.10:6878761::ATAT 18/3708)	-	Oct 12, 2018 (152)
69	ALFA	NC_000010.11 - 6836800	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
ss4212391136	NC_000010.11:6836799:ATAT:	NC_000010.11:6836799:ATATATAT:ATAT	(self)
3338558127	NC_000010.11:6836799:ATATATAT:ATAT	NC_000010.11:6836799:ATATATAT:ATAT	(self)
ss4212391135	NC_000010.11:6836799:AT:	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATAT	(self)
3338558127	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATAT	(self)
ss288994698, ss551996267, ss552233629, ss553398865	NC_000010.9:6918767::AT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATAT	(self)
ss663998220, ss1536640946, ss1706624262, ss1706624266, ss2030998866, ss3737031651, ss3786571954, ss3791765693, ss3796647474, ss3839505677, ss5196118085	NC_000010.10:6878761::AT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATAT	(self)
ss3063639234, ss3064458540, ss3649281872, ss3844971741, ss4212391124, ss5282805644, ss5478594466, ss5740923635, ss5849423010, ss5877607395	NC_000010.11:6836799::AT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATAT	(self)
3338558127	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATAT	(self)
ss3689216268	NC_000010.11:6836807::AT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATAT	(self)
ss287853904	NT_008705.16:6818761::AT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATAT	(self)
ss4212391128	NC_000010.11:6836799::ATATATATATAC… NC_000010.11:6836799::ATATATATATACATATGTATACAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATACATATGTATACATATATATAT	(self)
3338558127	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATACATATGTATACATATATATAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATACATATGTATACATATATATAT	(self)
ss1706624264, ss1706624269, ss3737031654, ss5196118084	NC_000010.10:6878761::ATAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATAT	(self)
ss4212391125, ss5478594468, ss5740923637	NC_000010.11:6836799::ATAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATAT	(self)
3338558127	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATAT	(self)
ss3689216267	NC_000010.11:6836807::ATAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATAT	(self)
ss4212391126	NC_000010.11:6836799::ATATAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATATAT	(self)
3338558127	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATATAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATATAT	(self)
ss4212391129	NC_000010.11:6836799::ATATATATATAT… NC_000010.11:6836799::ATATATATATATGCATATGTATATACATATGTATACAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATATGCATATGTATATACATATGTATACATATATATAT	(self)
ss4212391130	NC_000010.11:6836799::ATATATATATGC… NC_000010.11:6836799::ATATATATATGCAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATGCATATATATAT	(self)
3338558127	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATGCATATATATAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATGCATATATATAT	(self)
	NC_000010.11:6836799::ATATATATATGC… NC_000010.11:6836799::ATATATATATGCATATGTATATACATATGTATACACATGCATATGTATATACATATGTATACAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATGCATATGTATATACATATGTATACACATGCATATGTATATACATATGTATACATATATATAT	(self)
	NC_000010.11:6836799::ATATATATATGC… NC_000010.11:6836799::ATATATATATGCATATGTATATACATATGTATACACATGTATATACATATGTATACAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATGCATATGTATATACATATGTATACACATGTATATACATATGTATACATATATATAT	(self)
ss3737031653	NC_000010.10:6878761::ATATATATATGC… NC_000010.10:6878761::ATATATATATGCATATGTATATACATATGTATACAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATGCATATGTATATACATATGTATACATATATATAT	(self)
ss4212391131, ss5478594469	NC_000010.11:6836799::ATATATATATGC… NC_000010.11:6836799::ATATATATATGCATATGTATATACATATGTATACAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATGCATATGTATATACATATGTATACATATATATAT	(self)
3338558127	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATGCATATGTATATACATATGTATACATATATATAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATGCATATGTATATACATATGTATACATATATATAT	(self)
ss4212391132	NC_000010.11:6836799::ATATATATATGT… NC_000010.11:6836799::ATATATATATGTATATACATATGTATACAT	NC_000010.11:6836799:ATATATAT:ATAT… NC_000010.11:6836799:ATATATAT:ATATATATATGTATATACATATGTATACATATATATAT	(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 rs140133886

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
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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

rs140133886