Name: rs35991384
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.

rs35991384

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:35169330-35169346 (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)₇ / del(T)₄ / delTTT / delTT…
del(T)₇ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.09730 (1067/10966, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: UBE2MP1 : 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	10966	TTTTTTTTTTTTTTTTT=0.89011	TTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00301, TTTTTTTTTTTTTTTTTT=0.09730, TTTTTTTTTTTTTTTTTTT=0.00866, TTTTTTTTTTTTTTTTTTTT=0.00091, TTTTTTTTTTTTTTTTTTTTT=0.00000	0.851509	0.039434	0.109057	32
European	Sub	9426	TTTTTTTTTTTTTTTTT=0.8724	TTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0035, TTTTTTTTTTTTTTTTTT=0.1130, TTTTTTTTTTTTTTTTTTT=0.0101, TTTTTTTTTTTTTTTTTTTT=0.0011, TTTTTTTTTTTTTTTTTTTTT=0.0000	0.826711	0.046137	0.127152	32
African	Sub	854	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	46	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	808	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	44	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	38	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	6	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	60	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	338	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	24	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	220	TTTTTTTTTTTTTTTTT=0.991	TTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.009, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	0.981818	0.0	0.018182	0

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	10966	(T)₁₇=0.89011	del(T)₇=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00301, dupT=0.09730, dupTT=0.00866, dupTTT=0.00091, dup(T)₄=0.00000
Allele Frequency Aggregator	European	Sub	9426	(T)₁₇=0.8724	del(T)₇=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0035, dupT=0.1130, dupTT=0.0101, dupTTT=0.0011, dup(T)₄=0.0000
Allele Frequency Aggregator	African	Sub	854	(T)₁₇=1.000	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	338	(T)₁₇=1.000	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	220	(T)₁₇=0.991	del(T)₇=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.009, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	60	(T)₁₇=1.00	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	44	(T)₁₇=1.00	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	24	(T)₁₇=1.00	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

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.35169340_35169346del
GRCh38.p14 chr 16	NC_000016.10:g.35169343_35169346del
GRCh38.p14 chr 16	NC_000016.10:g.35169344_35169346del
GRCh38.p14 chr 16	NC_000016.10:g.35169345_35169346del
GRCh38.p14 chr 16	NC_000016.10:g.35169346del
GRCh38.p14 chr 16	NC_000016.10:g.35169346dup
GRCh38.p14 chr 16	NC_000016.10:g.35169345_35169346dup
GRCh38.p14 chr 16	NC_000016.10:g.35169344_35169346dup
GRCh38.p14 chr 16	NC_000016.10:g.35169343_35169346dup
GRCh38.p14 chr 16	NC_000016.10:g.35169337_35169346dup
GRCh37.p13 chr 16	NC_000016.9:g.34403711_34403717del
GRCh37.p13 chr 16	NC_000016.9:g.34403714_34403717del
GRCh37.p13 chr 16	NC_000016.9:g.34403715_34403717del
GRCh37.p13 chr 16	NC_000016.9:g.34403716_34403717del
GRCh37.p13 chr 16	NC_000016.9:g.34403717del
GRCh37.p13 chr 16	NC_000016.9:g.34403717dup
GRCh37.p13 chr 16	NC_000016.9:g.34403716_34403717dup
GRCh37.p13 chr 16	NC_000016.9:g.34403715_34403717dup
GRCh37.p13 chr 16	NC_000016.9:g.34403714_34403717dup
GRCh37.p13 chr 16	NC_000016.9:g.34403708_34403717dup

Gene: UBE2MP1, ubiquitin conjugating enzyme E2 M pseudogene 1 (minus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
UBE2MP1 transcript	NR_002837.1:n.	N/A	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)₁₇=	del(T)₇	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₁₀
GRCh38.p14 chr 16	NC_000016.10:g.35169330_35169346=	NC_000016.10:g.35169340_35169346del	NC_000016.10:g.35169343_35169346del	NC_000016.10:g.35169344_35169346del	NC_000016.10:g.35169345_35169346del	NC_000016.10:g.35169346del	NC_000016.10:g.35169346dup	NC_000016.10:g.35169345_35169346dup	NC_000016.10:g.35169344_35169346dup	NC_000016.10:g.35169343_35169346dup	NC_000016.10:g.35169337_35169346dup
GRCh37.p13 chr 16	NC_000016.9:g.34403701_34403717=	NC_000016.9:g.34403711_34403717del	NC_000016.9:g.34403714_34403717del	NC_000016.9:g.34403715_34403717del	NC_000016.9:g.34403716_34403717del	NC_000016.9:g.34403717del	NC_000016.9:g.34403717dup	NC_000016.9:g.34403716_34403717dup	NC_000016.9:g.34403715_34403717dup	NC_000016.9:g.34403714_34403717dup	NC_000016.9:g.34403708_34403717dup

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, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42811849	Mar 15, 2006 (126)
2	HUMANGENOME_JCVI	ss96712908	Oct 12, 2018 (152)
3	PJP	ss294887367	May 09, 2011 (137)
4	PJP	ss294887368	May 09, 2011 (135)
5	MCHAISSO	ss3063843958	Nov 08, 2017 (151)
6	URBANLAB	ss3650502557	Oct 12, 2018 (152)
7	EVA_DECODE	ss3699169267	Jul 13, 2019 (153)
8	EVA_DECODE	ss3699169268	Jul 13, 2019 (153)
9	EVA_DECODE	ss3699169269	Jul 13, 2019 (153)
10	EVA_DECODE	ss3699169270	Jul 13, 2019 (153)
11	EVA_DECODE	ss3699169271	Jul 13, 2019 (153)
12	EVA_DECODE	ss3699169272	Jul 13, 2019 (153)
13	EVA	ss3834552058	Apr 27, 2020 (154)
14	KOGIC	ss3977470877	Apr 27, 2020 (154)
15	KOGIC	ss3977470878	Apr 27, 2020 (154)
16	KOGIC	ss3977470879	Apr 27, 2020 (154)
17	GNOMAD	ss4300059801	Apr 26, 2021 (155)
18	GNOMAD	ss4300059802	Apr 26, 2021 (155)
19	GNOMAD	ss4300059803	Apr 26, 2021 (155)
20	GNOMAD	ss4300059804	Apr 26, 2021 (155)
21	GNOMAD	ss4300059806	Apr 26, 2021 (155)
22	GNOMAD	ss4300059807	Apr 26, 2021 (155)
23	GNOMAD	ss4300059808	Apr 26, 2021 (155)
24	GNOMAD	ss4300059809	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5219352234	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5219352235	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5219352236	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5219352237	Apr 26, 2021 (155)
29	1000G_HIGH_COVERAGE	ss5300779247	Oct 16, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5300779248	Oct 16, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5300779249	Oct 16, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5300779250	Oct 16, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5300779251	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5494160363	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5494160364	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5494160365	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5494160367	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5494160368	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5774133309	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5774133310	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5774133312	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5774133313	Oct 16, 2022 (156)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 488060138 (NC_000016.10:35169329::T 43309/126400) Row 488060139 (NC_000016.10:35169329::TT 5467/126388) Row 488060140 (NC_000016.10:35169329::TTT 255/126432)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 488060138 (NC_000016.10:35169329::T 43309/126400) Row 488060139 (NC_000016.10:35169329::TT 5467/126388) Row 488060140 (NC_000016.10:35169329::TTT 255/126432)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 488060138 (NC_000016.10:35169329::T 43309/126400) Row 488060139 (NC_000016.10:35169329::TT 5467/126388) Row 488060140 (NC_000016.10:35169329::TTT 255/126432)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 488060138 (NC_000016.10:35169329::T 43309/126400) Row 488060139 (NC_000016.10:35169329::TT 5467/126388) Row 488060140 (NC_000016.10:35169329::TTT 255/126432)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 488060138 (NC_000016.10:35169329::T 43309/126400) Row 488060139 (NC_000016.10:35169329::TT 5467/126388) Row 488060140 (NC_000016.10:35169329::TTT 255/126432)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 488060138 (NC_000016.10:35169329::T 43309/126400) Row 488060139 (NC_000016.10:35169329::TT 5467/126388) Row 488060140 (NC_000016.10:35169329::TTT 255/126432)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 488060138 (NC_000016.10:35169329::T 43309/126400) Row 488060139 (NC_000016.10:35169329::TT 5467/126388) Row 488060140 (NC_000016.10:35169329::TTT 255/126432)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 488060138 (NC_000016.10:35169329::T 43309/126400) Row 488060139 (NC_000016.10:35169329::TT 5467/126388) Row 488060140 (NC_000016.10:35169329::TTT 255/126432)...	-	Apr 26, 2021 (155)
51	Korean Genome Project Submission ignored due to conflicting rows: Row 33848878 (NC_000016.10:35169330::T 601/1820) Row 33848879 (NC_000016.10:35169329:T: 65/1820) Row 33848880 (NC_000016.10:35169330::TT 47/1820)	-	Apr 27, 2020 (154)
52	Korean Genome Project Submission ignored due to conflicting rows: Row 33848878 (NC_000016.10:35169330::T 601/1820) Row 33848879 (NC_000016.10:35169329:T: 65/1820) Row 33848880 (NC_000016.10:35169330::TT 47/1820)	-	Apr 27, 2020 (154)
53	Korean Genome Project Submission ignored due to conflicting rows: Row 33848878 (NC_000016.10:35169330::T 601/1820) Row 33848879 (NC_000016.10:35169329:T: 65/1820) Row 33848880 (NC_000016.10:35169330::TT 47/1820)	-	Apr 27, 2020 (154)
54	8.3KJPN Submission ignored due to conflicting rows: Row 77321541 (NC_000016.9:34403700::T 7159/16728) Row 77321542 (NC_000016.9:34403700::TT 194/16728) Row 77321543 (NC_000016.9:34403700:T: 85/16728)...	-	Apr 26, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 77321541 (NC_000016.9:34403700::T 7159/16728) Row 77321542 (NC_000016.9:34403700::TT 194/16728) Row 77321543 (NC_000016.9:34403700:T: 85/16728)...	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 77321541 (NC_000016.9:34403700::T 7159/16728) Row 77321542 (NC_000016.9:34403700::TT 194/16728) Row 77321543 (NC_000016.9:34403700:T: 85/16728)...	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 77321541 (NC_000016.9:34403700::T 7159/16728) Row 77321542 (NC_000016.9:34403700::TT 194/16728) Row 77321543 (NC_000016.9:34403700:T: 85/16728)...	-	Apr 26, 2021 (155)
58	14KJPN Submission ignored due to conflicting rows: Row 107970413 (NC_000016.10:35169329::T 12164/28246) Row 107970414 (NC_000016.10:35169329::TT 313/28246) Row 107970416 (NC_000016.10:35169329:T: 123/28246)...	-	Oct 16, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 107970413 (NC_000016.10:35169329::T 12164/28246) Row 107970414 (NC_000016.10:35169329::TT 313/28246) Row 107970416 (NC_000016.10:35169329:T: 123/28246)...	-	Oct 16, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 107970413 (NC_000016.10:35169329::T 12164/28246) Row 107970414 (NC_000016.10:35169329::TT 313/28246) Row 107970416 (NC_000016.10:35169329:T: 123/28246)...	-	Oct 16, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 107970413 (NC_000016.10:35169329::T 12164/28246) Row 107970414 (NC_000016.10:35169329::TT 313/28246) Row 107970416 (NC_000016.10:35169329:T: 123/28246)...	-	Oct 16, 2022 (156)
62	ALFA	NC_000016.10 - 35169330	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)
rs142472755	May 11, 2012 (137)
rs149789924	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
14800207654	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4300059809	NC_000016.10:35169329:TTTT:	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4300059808	NC_000016.10:35169329:TTT:	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
14800207654	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3699169267, ss4300059807, ss5300779251, ss5494160367	NC_000016.10:35169329:TT:	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
14800207654	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5219352236	NC_000016.9:34403700:T:	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3977470878, ss4300059806, ss5300779249, ss5494160364, ss5774133312	NC_000016.10:35169329:T:	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
14800207654	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3699169268	NC_000016.10:35169330:T:	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss294887367	NC_000016.8:34261202::T	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss294887368	NC_000016.8:34261218::T	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3834552058, ss5219352234	NC_000016.9:34403700::T	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3063843958, ss3650502557, ss4300059801, ss5300779247, ss5494160363, ss5774133309	NC_000016.10:35169329::T	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
14800207654	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3977470877	NC_000016.10:35169330::T	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3699169269	NC_000016.10:35169331::T	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss42811849	NT_024773.11:230550::T	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss96712908	NT_024773.11:230567::T	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5219352235	NC_000016.9:34403700::TT	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4300059802, ss5300779248, ss5494160365, ss5774133310	NC_000016.10:35169329::TT	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
14800207654	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3977470879	NC_000016.10:35169330::TT	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3699169270	NC_000016.10:35169331::TT	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5219352237	NC_000016.9:34403700::TTT	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4300059803, ss5300779250, ss5494160368, ss5774133313	NC_000016.10:35169329::TTT	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
14800207654	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3699169271	NC_000016.10:35169331::TTT	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4300059804	NC_000016.10:35169329::TTTT	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
14800207654	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3699169272	NC_000016.10:35169331::TTTTTTTTTT	NC_000016.10:35169329:TTTTTTTTTTTT… NC_000016.10:35169329:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs35991384

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

rs35991384