Name: rs36111419
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.

rs36111419

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:3694001-3694017 (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: delAA=0.3471 (1857/5350, ALFA)
(A)₁₇=0.2093 (1048/5008, 1000G)
delAA=0.47 (19/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TRAP1 : 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	5350	AAAAAAAAAAAAAAAAA=0.6333	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.3471, AAAAAAAAAAAAAAAA=0.0196, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	0.505653	0.203509	0.290838	32
European	Sub	5192	AAAAAAAAAAAAAAAAA=0.6229	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.3571, AAAAAAAAAAAAAAAA=0.0200, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	0.490551	0.209489	0.29996	32
African	Sub	30	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	AAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
African American	Sub	30	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	0	AAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	10	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	66	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	8	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	44	AAAAAAAAAAAAAAAAA=0.91	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.07, AAAAAAAAAAAAAAAA=0.02, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	0.952381	0.047619	0.0	12

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	5350	(A)₁₇=0.6333	del(A)₄=0.0000, delAAA=0.0000, delAA=0.3471, delA=0.0196, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	5192	(A)₁₇=0.6229	del(A)₄=0.0000, delAAA=0.0000, delAA=0.3571, delA=0.0200, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	66	(A)₁₇=1.00	del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Other	Sub	44	(A)₁₇=0.91	del(A)₄=0.00, delAAA=0.00, delAA=0.07, delA=0.02, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	African	Sub	30	(A)₁₇=1.00	del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	10	(A)₁₇=1.0	del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	South Asian	Sub	8	(A)₁₇=1.0	del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	Asian	Sub	0	(A)₁₇=0	del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0
1000Genomes	Global	Study-wide	5008	(A)₁₇=0.2093	delAA=0.7907
1000Genomes	African	Sub	1322	(A)₁₇=0.1059	delAA=0.8941
1000Genomes	East Asian	Sub	1008	(A)₁₇=0.1329	delAA=0.8671
1000Genomes	Europe	Sub	1006	(A)₁₇=0.3360	delAA=0.6640
1000Genomes	South Asian	Sub	978	(A)₁₇=0.222	delAA=0.778
1000Genomes	American	Sub	694	(A)₁₇=0.316	delAA=0.684
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₇=0.53	delAA=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 16	NC_000016.10:g.3694013_3694017del
GRCh38.p14 chr 16	NC_000016.10:g.3694014_3694017del
GRCh38.p14 chr 16	NC_000016.10:g.3694015_3694017del
GRCh38.p14 chr 16	NC_000016.10:g.3694016_3694017del
GRCh38.p14 chr 16	NC_000016.10:g.3694017del
GRCh38.p14 chr 16	NC_000016.10:g.3694017dup
GRCh38.p14 chr 16	NC_000016.10:g.3694016_3694017dup
GRCh37.p13 chr 16	NC_000016.9:g.3744014_3744018del
GRCh37.p13 chr 16	NC_000016.9:g.3744015_3744018del
GRCh37.p13 chr 16	NC_000016.9:g.3744016_3744018del
GRCh37.p13 chr 16	NC_000016.9:g.3744017_3744018del
GRCh37.p13 chr 16	NC_000016.9:g.3744018del
GRCh37.p13 chr 16	NC_000016.9:g.3744018dup
GRCh37.p13 chr 16	NC_000016.9:g.3744017_3744018dup
TRAP1 RefSeqGene	NG_033088.1:g.28593_28597del
TRAP1 RefSeqGene	NG_033088.1:g.28594_28597del
TRAP1 RefSeqGene	NG_033088.1:g.28595_28597del
TRAP1 RefSeqGene	NG_033088.1:g.28596_28597del
TRAP1 RefSeqGene	NG_033088.1:g.28597del
TRAP1 RefSeqGene	NG_033088.1:g.28597dup
TRAP1 RefSeqGene	NG_033088.1:g.28596_28597dup

Gene: TRAP1, TNF receptor associated protein 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TRAP1 transcript variant 2	NM_001272049.2:c.89-4868_… NM_001272049.2:c.89-4868_89-4864del	N/A	Intron Variant
TRAP1 transcript variant 1	NM_016292.3:c.89-3020_89-… NM_016292.3:c.89-3020_89-3016del	N/A	Intron Variant
TRAP1 transcript variant X1	XM_011522345.3:c.-332-302… XM_011522345.3:c.-332-3020_-332-3016del	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 16	NC_000016.10:g.3694001_3694017=	NC_000016.10:g.3694013_3694017del	NC_000016.10:g.3694014_3694017del	NC_000016.10:g.3694015_3694017del	NC_000016.10:g.3694016_3694017del	NC_000016.10:g.3694017del	NC_000016.10:g.3694017dup	NC_000016.10:g.3694016_3694017dup
GRCh37.p13 chr 16	NC_000016.9:g.3744002_3744018=	NC_000016.9:g.3744014_3744018del	NC_000016.9:g.3744015_3744018del	NC_000016.9:g.3744016_3744018del	NC_000016.9:g.3744017_3744018del	NC_000016.9:g.3744018del	NC_000016.9:g.3744018dup	NC_000016.9:g.3744017_3744018dup
TRAP1 RefSeqGene	NG_033088.1:g.28581_28597=	NG_033088.1:g.28593_28597del	NG_033088.1:g.28594_28597del	NG_033088.1:g.28595_28597del	NG_033088.1:g.28596_28597del	NG_033088.1:g.28597del	NG_033088.1:g.28597dup	NG_033088.1:g.28596_28597dup
TRAP1 transcript variant 2	NM_001272049.1:c.89-4864=	NM_001272049.1:c.89-4868_89-4864del	NM_001272049.1:c.89-4867_89-4864del	NM_001272049.1:c.89-4866_89-4864del	NM_001272049.1:c.89-4865_89-4864del	NM_001272049.1:c.89-4864del	NM_001272049.1:c.89-4864dup	NM_001272049.1:c.89-4865_89-4864dup
TRAP1 transcript variant 2	NM_001272049.2:c.89-4864=	NM_001272049.2:c.89-4868_89-4864del	NM_001272049.2:c.89-4867_89-4864del	NM_001272049.2:c.89-4866_89-4864del	NM_001272049.2:c.89-4865_89-4864del	NM_001272049.2:c.89-4864del	NM_001272049.2:c.89-4864dup	NM_001272049.2:c.89-4865_89-4864dup
TRAP1 transcript variant 1	NM_016292.2:c.89-3016=	NM_016292.2:c.89-3020_89-3016del	NM_016292.2:c.89-3019_89-3016del	NM_016292.2:c.89-3018_89-3016del	NM_016292.2:c.89-3017_89-3016del	NM_016292.2:c.89-3016del	NM_016292.2:c.89-3016dup	NM_016292.2:c.89-3017_89-3016dup
TRAP1 transcript variant 1	NM_016292.3:c.89-3016=	NM_016292.3:c.89-3020_89-3016del	NM_016292.3:c.89-3019_89-3016del	NM_016292.3:c.89-3018_89-3016del	NM_016292.3:c.89-3017_89-3016del	NM_016292.3:c.89-3016del	NM_016292.3:c.89-3016dup	NM_016292.3:c.89-3017_89-3016dup
TRAP1 transcript variant X1	XM_011522345.3:c.-332-3016=	XM_011522345.3:c.-332-3020_-332-3016del	XM_011522345.3:c.-332-3019_-332-3016del	XM_011522345.3:c.-332-3018_-332-3016del	XM_011522345.3:c.-332-3017_-332-3016del	XM_011522345.3:c.-332-3016del	XM_011522345.3:c.-332-3016dup	XM_011522345.3:c.-332-3017_-332-3016dup

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#.

54 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40732326	Mar 15, 2006 (126)
2	HGSV	ss81064256	Dec 15, 2007 (130)
3	HGSV	ss83669313	Dec 15, 2007 (130)
4	HUMANGENOME_JCVI	ss95670046	Feb 05, 2009 (130)
5	BUSHMAN	ss193403297	Mar 15, 2016 (147)
6	PJP	ss294878015	May 31, 2013 (142)
7	SSMP	ss664313649	Apr 01, 2015 (144)
8	BILGI_BIOE	ss666661769	Apr 25, 2013 (138)
9	SSIP	ss947350834	Aug 21, 2014 (142)
10	1000GENOMES	ss1375477934	Aug 21, 2014 (142)
11	EVA_GENOME_DK	ss1574917314	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1708446347	Apr 01, 2015 (144)
13	EVA_UK10K_TWINSUK	ss1708446349	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1710686579	Apr 01, 2015 (144)
15	EVA_UK10K_ALSPAC	ss1710686589	Apr 01, 2015 (144)
16	HAMMER_LAB	ss1808385345	Sep 08, 2015 (146)
17	SYSTEMSBIOZJU	ss2628790707	Nov 08, 2017 (151)
18	SWEGEN	ss3013951344	Nov 08, 2017 (151)
19	MCHAISSO	ss3063834467	Nov 08, 2017 (151)
20	MCHAISSO	ss3064673868	Nov 08, 2017 (151)
21	MCHAISSO	ss3065607215	Nov 08, 2017 (151)
22	URBANLAB	ss3650446823	Oct 12, 2018 (152)
23	EVA_DECODE	ss3698699242	Jul 13, 2019 (153)
24	EVA_DECODE	ss3698699243	Jul 13, 2019 (153)
25	EVA_DECODE	ss3698699244	Jul 13, 2019 (153)
26	EVA_DECODE	ss3698699245	Jul 13, 2019 (153)
27	INMEGENXS	ss3745612663	Jul 13, 2019 (153)
28	INMEGENXS	ss3745612664	Jul 13, 2019 (153)
29	PACBIO	ss3787960746	Jul 13, 2019 (153)
30	PACBIO	ss3792955843	Jul 13, 2019 (153)
31	PACBIO	ss3797840737	Jul 13, 2019 (153)
32	KHV_HUMAN_GENOMES	ss3818894177	Jul 13, 2019 (153)
33	EVA	ss3834437364	Apr 27, 2020 (154)
34	EVA	ss3840822860	Apr 27, 2020 (154)
35	EVA	ss3846313594	Apr 27, 2020 (154)
36	GNOMAD	ss4295752407	Apr 27, 2021 (155)
37	GNOMAD	ss4295752409	Apr 27, 2021 (155)
38	GNOMAD	ss4295752410	Apr 27, 2021 (155)
39	GNOMAD	ss4295752411	Apr 27, 2021 (155)
40	GNOMAD	ss4295752412	Apr 27, 2021 (155)
41	GNOMAD	ss4295752413	Apr 27, 2021 (155)
42	TOMMO_GENOMICS	ss5218102153	Apr 27, 2021 (155)
43	TOMMO_GENOMICS	ss5218102154	Apr 27, 2021 (155)
44	1000G_HIGH_COVERAGE	ss5299882618	Oct 17, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5299882619	Oct 17, 2022 (156)
46	HUGCELL_USP	ss5493435795	Oct 17, 2022 (156)
47	HUGCELL_USP	ss5493435796	Oct 17, 2022 (156)
48	HUGCELL_USP	ss5493435797	Oct 17, 2022 (156)
49	TOMMO_GENOMICS	ss5772487239	Oct 17, 2022 (156)
50	TOMMO_GENOMICS	ss5772487240	Oct 17, 2022 (156)
51	EVA	ss5846005841	Oct 17, 2022 (156)
52	EVA	ss5846005842	Oct 17, 2022 (156)
53	EVA	ss5851459969	Oct 17, 2022 (156)
54	EVA	ss5897997033	Oct 17, 2022 (156)
55	1000Genomes	NC_000016.9 - 3744002	Oct 12, 2018 (152)
56	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 37876401 (NC_000016.9:3744002:A: 2926/3854) Row 37876402 (NC_000016.9:3744001:AAA: 254/3854)	-	Oct 12, 2018 (152)
57	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 37876401 (NC_000016.9:3744002:A: 2926/3854) Row 37876402 (NC_000016.9:3744001:AAA: 254/3854)	-	Oct 12, 2018 (152)
58	The Danish reference pan genome	NC_000016.9 - 3744002	Apr 27, 2020 (154)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480823062 (NC_000016.10:3694000::A 94/122210) Row 480823064 (NC_000016.10:3694000:A: 1841/122042) Row 480823065 (NC_000016.10:3694000:AA: 88610/121970)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480823062 (NC_000016.10:3694000::A 94/122210) Row 480823064 (NC_000016.10:3694000:A: 1841/122042) Row 480823065 (NC_000016.10:3694000:AA: 88610/121970)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480823062 (NC_000016.10:3694000::A 94/122210) Row 480823064 (NC_000016.10:3694000:A: 1841/122042) Row 480823065 (NC_000016.10:3694000:AA: 88610/121970)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480823062 (NC_000016.10:3694000::A 94/122210) Row 480823064 (NC_000016.10:3694000:A: 1841/122042) Row 480823065 (NC_000016.10:3694000:AA: 88610/121970)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480823062 (NC_000016.10:3694000::A 94/122210) Row 480823064 (NC_000016.10:3694000:A: 1841/122042) Row 480823065 (NC_000016.10:3694000:AA: 88610/121970)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480823062 (NC_000016.10:3694000::A 94/122210) Row 480823064 (NC_000016.10:3694000:A: 1841/122042) Row 480823065 (NC_000016.10:3694000:AA: 88610/121970)...	-	Apr 27, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 76071460 (NC_000016.9:3744001:AA: 14291/16696) Row 76071461 (NC_000016.9:3744001:A: 22/16696)	-	Apr 27, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 76071460 (NC_000016.9:3744001:AA: 14291/16696) Row 76071461 (NC_000016.9:3744001:A: 22/16696)	-	Apr 27, 2021 (155)
67	14KJPN Submission ignored due to conflicting rows: Row 106324343 (NC_000016.10:3694000:AA: 24375/28246) Row 106324344 (NC_000016.10:3694000:A: 25/28246)	-	Oct 17, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 106324343 (NC_000016.10:3694000:AA: 24375/28246) Row 106324344 (NC_000016.10:3694000:A: 25/28246)	-	Oct 17, 2022 (156)
69	UK 10K study - Twins Submission ignored due to conflicting rows: Row 37876401 (NC_000016.9:3744002:A: 2818/3708) Row 37876402 (NC_000016.9:3744001:AAA: 210/3708)	-	Oct 12, 2018 (152)
70	UK 10K study - Twins Submission ignored due to conflicting rows: Row 37876401 (NC_000016.9:3744002:A: 2818/3708) Row 37876402 (NC_000016.9:3744001:AAA: 210/3708)	-	Oct 12, 2018 (152)
71	ALFA	NC_000016.10 - 3694001	Apr 27, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs59095274	May 25, 2008 (130)
rs386384078	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4295752413	NC_000016.10:3694000:AAAAA:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3698699245, ss4295752412, ss5493435797	NC_000016.10:3694000:AAAA:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
9303942922	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss1708446347, ss1708446349, ss3013951344, ss5846005842	NC_000016.9:3744001:AAA:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4295752411	NC_000016.10:3694000:AAA:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
9303942922	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3698699244	NC_000016.10:3694001:AAA:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss294878015	NC_000016.8:3684002:AA:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss81064256, ss83669313	NC_000016.8:3684017:AA:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
68220812, 512831, ss664313649, ss666661769, ss1375477934, ss1574917314, ss1808385345, ss2628790707, ss3745612663, ss3787960746, ss3792955843, ss3797840737, ss3834437364, ss3840822860, ss5218102153, ss5846005841	NC_000016.9:3744001:AA:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss947350834, ss1710686579, ss1710686589, ss3745612664	NC_000016.9:3744002:AA:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3063834467, ss3064673868, ss3065607215, ss3650446823, ss3818894177, ss3846313594, ss4295752410, ss5299882618, ss5493435795, ss5772487239, ss5851459969, ss5897997033	NC_000016.10:3694000:AA:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
9303942922	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3698699243	NC_000016.10:3694002:AA:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss193403297	NT_010393.16:3684001:AA:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss95670046	NT_010393.16:3684016:AA:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss5218102154	NC_000016.9:3744001:A:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
	NC_000016.9:3744002:A:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4295752409, ss5299882619, ss5493435796, ss5772487240	NC_000016.10:3694000:A:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
9303942922	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3698699242	NC_000016.10:3694003:A:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss40732326	NT_010393.16:3684017:A:	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4295752407	NC_000016.10:3694000::A	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
9303942922	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss40732326	NT_010393.16:3684017:A:AA	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
9303942922	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000016.10:3694000:AAAAAAAAAAAAA… NC_000016.10:3694000: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 rs36111419

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

rs36111419