Name: rs66751016
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.

rs66751016

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:30891531-30891548 (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(T)₁₀ / del(T)₇ / del(T)₅ / del…
del(T)₁₀ / del(T)₇ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.05330 (663/12438, ALFA)
delT=0.35 (14/40, GENOME_DK)
dupT=0.2 (2/8, KOREAN)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TEX26-AS1 : 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	12438	TTTTTTTTTTTTTTTTTT=0.91807	TTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.05330, TTTTTTTTTTTTTTTTTTT=0.02830, TTTTTTTTTTTTTTTTTTTTT=0.00032, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000	0.90886	0.01135	0.07979	32
European	Sub	10666	TTTTTTTTTTTTTTTTTT=0.90446	TTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.06216, TTTTTTTTTTTTTTTTTTT=0.03300, TTTTTTTTTTTTTTTTTTTTT=0.00038, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000	0.892765	0.013355	0.093881	32
African	Sub	950	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	28	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	922	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	42	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	32	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	10	TTTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	66	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	418	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	44	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	252	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=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	12438	(T)₁₈=0.91807	del(T)₁₀=0.00000, del(T)₇=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.05330, dupT=0.02830, dupTT=0.00000, dupTTT=0.00032, dup(T)₄=0.00000
Allele Frequency Aggregator	European	Sub	10666	(T)₁₈=0.90446	del(T)₁₀=0.00000, del(T)₇=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.06216, dupT=0.03300, dupTT=0.00000, dupTTT=0.00038, dup(T)₄=0.00000
Allele Frequency Aggregator	African	Sub	950	(T)₁₈=1.000	del(T)₁₀=0.000, del(T)₇=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	418	(T)₁₈=1.000	del(T)₁₀=0.000, del(T)₇=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Other	Sub	252	(T)₁₈=1.000	del(T)₁₀=0.000, del(T)₇=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	66	(T)₁₈=1.00	del(T)₁₀=0.00, del(T)₇=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	44	(T)₁₈=1.00	del(T)₁₀=0.00, del(T)₇=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Asian	Sub	42	(T)₁₈=1.00	del(T)₁₀=0.00, del(T)₇=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
The Danish reference pan genome	Danish	Study-wide	40	(T)₁₈=0.65	delT=0.35
KOREAN population from KRGDB	KOREAN	Study-wide	8	- No frequency provided	dupT=0.2

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 13	NC_000013.11:g.30891539_30891548del
GRCh38.p14 chr 13	NC_000013.11:g.30891542_30891548del
GRCh38.p14 chr 13	NC_000013.11:g.30891544_30891548del
GRCh38.p14 chr 13	NC_000013.11:g.30891545_30891548del
GRCh38.p14 chr 13	NC_000013.11:g.30891546_30891548del
GRCh38.p14 chr 13	NC_000013.11:g.30891547_30891548del
GRCh38.p14 chr 13	NC_000013.11:g.30891548del
GRCh38.p14 chr 13	NC_000013.11:g.30891548dup
GRCh38.p14 chr 13	NC_000013.11:g.30891547_30891548dup
GRCh38.p14 chr 13	NC_000013.11:g.30891546_30891548dup
GRCh38.p14 chr 13	NC_000013.11:g.30891545_30891548dup
GRCh38.p14 chr 13	NC_000013.11:g.30891539_30891548dup
GRCh37.p13 chr 13	NC_000013.10:g.31465676_31465685del
GRCh37.p13 chr 13	NC_000013.10:g.31465679_31465685del
GRCh37.p13 chr 13	NC_000013.10:g.31465681_31465685del
GRCh37.p13 chr 13	NC_000013.10:g.31465682_31465685del
GRCh37.p13 chr 13	NC_000013.10:g.31465683_31465685del
GRCh37.p13 chr 13	NC_000013.10:g.31465684_31465685del
GRCh37.p13 chr 13	NC_000013.10:g.31465685del
GRCh37.p13 chr 13	NC_000013.10:g.31465685dup
GRCh37.p13 chr 13	NC_000013.10:g.31465684_31465685dup
GRCh37.p13 chr 13	NC_000013.10:g.31465683_31465685dup
GRCh37.p13 chr 13	NC_000013.10:g.31465682_31465685dup
GRCh37.p13 chr 13	NC_000013.10:g.31465676_31465685dup

Gene: TEX26-AS1, TEX26 antisense RNA 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TEX26-AS1 transcript variant 1	NR_038287.1:n.	N/A	Intron Variant
TEX26-AS1 transcript variant 2	NR_038288.1:n.	N/A	Genic Downstream Transcript 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	(T)₁₈=	del(T)₁₀	del(T)₇	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₁₀
GRCh38.p14 chr 13	NC_000013.11:g.30891531_30891548=	NC_000013.11:g.30891539_30891548del	NC_000013.11:g.30891542_30891548del	NC_000013.11:g.30891544_30891548del	NC_000013.11:g.30891545_30891548del	NC_000013.11:g.30891546_30891548del	NC_000013.11:g.30891547_30891548del	NC_000013.11:g.30891548del	NC_000013.11:g.30891548dup	NC_000013.11:g.30891547_30891548dup	NC_000013.11:g.30891546_30891548dup	NC_000013.11:g.30891545_30891548dup	NC_000013.11:g.30891539_30891548dup
GRCh37.p13 chr 13	NC_000013.10:g.31465668_31465685=	NC_000013.10:g.31465676_31465685del	NC_000013.10:g.31465679_31465685del	NC_000013.10:g.31465681_31465685del	NC_000013.10:g.31465682_31465685del	NC_000013.10:g.31465683_31465685del	NC_000013.10:g.31465684_31465685del	NC_000013.10:g.31465685del	NC_000013.10:g.31465685dup	NC_000013.10:g.31465684_31465685dup	NC_000013.10:g.31465683_31465685dup	NC_000013.10:g.31465682_31465685dup	NC_000013.10:g.31465676_31465685dup

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#.

38 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95616269	Dec 05, 2013 (142)
2	GMI	ss289169193	May 04, 2012 (137)
3	PJP	ss294790253	May 09, 2011 (137)
4	SSIP	ss947311761	Oct 12, 2018 (152)
5	EVA_GENOME_DK	ss1574617401	Apr 01, 2015 (144)
6	SWEGEN	ss3010801770	Nov 08, 2017 (151)
7	MCHAISSO	ss3063758914	Nov 08, 2017 (151)
8	EVA_DECODE	ss3695025732	Jul 13, 2019 (153)
9	EVA_DECODE	ss3695025734	Jul 13, 2019 (153)
10	EVA_DECODE	ss3695025735	Jul 13, 2019 (153)
11	EVA_DECODE	ss3695025736	Jul 13, 2019 (153)
12	PACBIO	ss3787419802	Jul 13, 2019 (153)
13	PACBIO	ss3792491860	Jul 13, 2019 (153)
14	PACBIO	ss3797375611	Jul 13, 2019 (153)
15	EVA	ss3833476654	Apr 27, 2020 (154)
16	KRGDB	ss3928520986	Apr 27, 2020 (154)
17	GNOMAD	ss4263536065	Apr 26, 2021 (155)
18	GNOMAD	ss4263536066	Apr 26, 2021 (155)
19	GNOMAD	ss4263536067	Apr 26, 2021 (155)
20	GNOMAD	ss4263536069	Apr 26, 2021 (155)
21	GNOMAD	ss4263536070	Apr 26, 2021 (155)
22	GNOMAD	ss4263536071	Apr 26, 2021 (155)
23	GNOMAD	ss4263536072	Apr 26, 2021 (155)
24	GNOMAD	ss4263536073	Apr 26, 2021 (155)
25	GNOMAD	ss4263536074	Apr 26, 2021 (155)
26	GNOMAD	ss4263536075	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5209391047	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5209391048	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5209391049	Apr 26, 2021 (155)
30	1000G_HIGH_COVERAGE	ss5293267382	Oct 16, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5293267383	Oct 16, 2022 (156)
32	HUGCELL_USP	ss5487677070	Oct 16, 2022 (156)
33	HUGCELL_USP	ss5487677071	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5487677072	Oct 16, 2022 (156)
35	TOMMO_GENOMICS	ss5761094665	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5761094666	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5761094667	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5761094668	Oct 16, 2022 (156)
39	The Danish reference pan genome	NC_000013.10 - 31465668	Apr 27, 2020 (154)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 426859810 (NC_000013.11:30891530::T 23920/123810) Row 426859811 (NC_000013.11:30891530::TT 339/123818) Row 426859812 (NC_000013.11:30891530::TTT 25/123828)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 426859810 (NC_000013.11:30891530::T 23920/123810) Row 426859811 (NC_000013.11:30891530::TT 339/123818) Row 426859812 (NC_000013.11:30891530::TTT 25/123828)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 426859810 (NC_000013.11:30891530::T 23920/123810) Row 426859811 (NC_000013.11:30891530::TT 339/123818) Row 426859812 (NC_000013.11:30891530::TTT 25/123828)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 426859810 (NC_000013.11:30891530::T 23920/123810) Row 426859811 (NC_000013.11:30891530::TT 339/123818) Row 426859812 (NC_000013.11:30891530::TTT 25/123828)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 426859810 (NC_000013.11:30891530::T 23920/123810) Row 426859811 (NC_000013.11:30891530::TT 339/123818) Row 426859812 (NC_000013.11:30891530::TTT 25/123828)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 426859810 (NC_000013.11:30891530::T 23920/123810) Row 426859811 (NC_000013.11:30891530::TT 339/123818) Row 426859812 (NC_000013.11:30891530::TTT 25/123828)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 426859810 (NC_000013.11:30891530::T 23920/123810) Row 426859811 (NC_000013.11:30891530::TT 339/123818) Row 426859812 (NC_000013.11:30891530::TTT 25/123828)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 426859810 (NC_000013.11:30891530::T 23920/123810) Row 426859811 (NC_000013.11:30891530::TT 339/123818) Row 426859812 (NC_000013.11:30891530::TTT 25/123828)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 426859810 (NC_000013.11:30891530::T 23920/123810) Row 426859811 (NC_000013.11:30891530::TT 339/123818) Row 426859812 (NC_000013.11:30891530::TTT 25/123828)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 426859810 (NC_000013.11:30891530::T 23920/123810) Row 426859811 (NC_000013.11:30891530::TT 339/123818) Row 426859812 (NC_000013.11:30891530::TTT 25/123828)...	-	Apr 26, 2021 (155)
50	KOREAN population from KRGDB	NC_000013.10 - 31465668	Apr 27, 2020 (154)
51	8.3KJPN Submission ignored due to conflicting rows: Row 67360354 (NC_000013.10:31465667::T 3749/16720) Row 67360355 (NC_000013.10:31465667:T: 28/16720) Row 67360356 (NC_000013.10:31465667::TT 11/16720)	-	Apr 26, 2021 (155)
52	8.3KJPN Submission ignored due to conflicting rows: Row 67360354 (NC_000013.10:31465667::T 3749/16720) Row 67360355 (NC_000013.10:31465667:T: 28/16720) Row 67360356 (NC_000013.10:31465667::TT 11/16720)	-	Apr 26, 2021 (155)
53	8.3KJPN Submission ignored due to conflicting rows: Row 67360354 (NC_000013.10:31465667::T 3749/16720) Row 67360355 (NC_000013.10:31465667:T: 28/16720) Row 67360356 (NC_000013.10:31465667::TT 11/16720)	-	Apr 26, 2021 (155)
54	14KJPN Submission ignored due to conflicting rows: Row 94931769 (NC_000013.11:30891530::T 6578/28256) Row 94931770 (NC_000013.11:30891530:T: 32/28256) Row 94931771 (NC_000013.11:30891530::TT 8/28256)...	-	Oct 16, 2022 (156)
55	14KJPN Submission ignored due to conflicting rows: Row 94931769 (NC_000013.11:30891530::T 6578/28256) Row 94931770 (NC_000013.11:30891530:T: 32/28256) Row 94931771 (NC_000013.11:30891530::TT 8/28256)...	-	Oct 16, 2022 (156)
56	14KJPN Submission ignored due to conflicting rows: Row 94931769 (NC_000013.11:30891530::T 6578/28256) Row 94931770 (NC_000013.11:30891530:T: 32/28256) Row 94931771 (NC_000013.11:30891530::TT 8/28256)...	-	Oct 16, 2022 (156)
57	14KJPN Submission ignored due to conflicting rows: Row 94931769 (NC_000013.11:30891530::T 6578/28256) Row 94931770 (NC_000013.11:30891530:T: 32/28256) Row 94931771 (NC_000013.11:30891530::TT 8/28256)...	-	Oct 16, 2022 (156)
58	ALFA	NC_000013.11 - 30891531	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).

Associated ID	History Updated (Build)
rs66751017	Feb 26, 2009 (130)
rs67490445	May 11, 2012 (137)
rs67490446	Feb 27, 2009 (130)
rs71093098	May 11, 2012 (137)
rs398022180	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4263536075	NC_000013.11:30891530:TTTTTTTTTT:	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
12759334799	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTT	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
ss4263536074	NC_000013.11:30891530:TTTTTTT:	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
12759334799	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4263536073	NC_000013.11:30891530:TTTTT:	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4263536072	NC_000013.11:30891530:TTTT:	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4263536071	NC_000013.11:30891530:TTT:	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
12759334799	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3695025732, ss4263536070	NC_000013.11:30891530:TT:	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
12759334799	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss294790253	NC_000013.9:30363684:T:	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
396386, ss1574617401, ss3010801770, ss3787419802, ss3792491860, ss3797375611, ss5209391048	NC_000013.10:31465667:T:	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4263536069, ss5293267383, ss5487677070, ss5761094666	NC_000013.11:30891530:T:	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
12759334799	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3695025734	NC_000013.11:30891531:T:	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss95616269	NT_024524.14:12445684:T:	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss289169193	NC_000013.9:30363685::T	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
35698380, ss3833476654, ss3928520986, ss5209391047	NC_000013.10:31465667::T	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss947311761	NC_000013.10:31465668::T	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3063758914, ss4263536065, ss5293267382, ss5487677071, ss5761094665	NC_000013.11:30891530::T	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
12759334799	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3695025735	NC_000013.11:30891532::T	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5209391049	NC_000013.10:31465667::TT	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4263536066, ss5487677072, ss5761094667	NC_000013.11:30891530::TT	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
12759334799	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4263536067, ss5761094668	NC_000013.11:30891530::TTT	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
12759334799	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
12759334799	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3695025736	NC_000013.11:30891532::TTTTTTTTTT	NC_000013.11:30891530:TTTTTTTTTTTT… NC_000013.11:30891530:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs66751016

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

rs66751016