Name: rs145357823
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.

rs145357823

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:77991715-77991731 (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: delGTGT / delGT / dupGT / dupGTGT …
delGTGT / delGT / dupGT / dupGTGT / dup(GT)₃
Variation Type: Indel Insertion and Deletion
Frequency: dupGT=0.03428 (498/14526, ALFA)
(TG)₈T=0.036 (9/253, 1000G)
dupGT=0.15 (6/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC01069 : 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	14526	TGTGTGTGTGTGTGTGT=0.96090	TGTGTGTGTGTGT=0.00021, TGTGTGTGTGTGTGT=0.00172, TGTGTGTGTGTGTGTGTGT=0.03428, TGTGTGTGTGTGTGTGTGTGT=0.00289, TGTGTGTGTGTGTGTGTGTGTGT=0.00000	0.935094	0.003892	0.061015	26
European	Sub	12044	TGTGTGTGTGTGTGTGT=0.95433	TGTGTGTGTGTGT=0.00025, TGTGTGTGTGTGTGT=0.00058, TGTGTGTGTGTGTGTGTGT=0.04135, TGTGTGTGTGTGTGTGTGTGT=0.00349, TGTGTGTGTGTGTGTGTGTGTGT=0.00000	0.921789	0.004689	0.073522	18
African	Sub	1642	TGTGTGTGTGTGTGTGT=0.9909	TGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGT=0.0091, TGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	58	TGTGTGTGTGTGTGTGT=0.95	TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.05, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1584	TGTGTGTGTGTGTGTGT=0.9924	TGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGT=0.0076, TGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	20	TGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	14	TGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	6	TGTGTGTGTGTGTGTGT=1.0	TGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	94	TGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	352	TGTGTGTGTGTGTGTGT=1.000	TGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	58	TGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other	Sub	316	TGTGTGTGTGTGTGTGT=0.991	TGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.009, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	14526	(TG)₈T=0.96090	delGTGT=0.00021, delGT=0.00172, dupGT=0.03428, dupGTGT=0.00289, dup(GT)₃=0.00000
Allele Frequency Aggregator	European	Sub	12044	(TG)₈T=0.95433	delGTGT=0.00025, delGT=0.00058, dupGT=0.04135, dupGTGT=0.00349, dup(GT)₃=0.00000
Allele Frequency Aggregator	African	Sub	1642	(TG)₈T=0.9909	delGTGT=0.0000, delGT=0.0091, dupGT=0.0000, dupGTGT=0.0000, dup(GT)₃=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	352	(TG)₈T=1.000	delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000
Allele Frequency Aggregator	Other	Sub	316	(TG)₈T=0.991	delGTGT=0.000, delGT=0.009, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000
Allele Frequency Aggregator	Latin American 1	Sub	94	(TG)₈T=1.00	delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00
Allele Frequency Aggregator	South Asian	Sub	58	(TG)₈T=1.00	delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00
Allele Frequency Aggregator	Asian	Sub	20	(TG)₈T=1.00	delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00
1000Genomes	Global	Study-wide	253	(TG)₈T=0.036	delGT=0.964
1000Genomes	African	Sub	217	(TG)₈T=0.009	delGT=0.991
1000Genomes	American	Sub	24	(TG)₈T=0.04	delGT=0.96
1000Genomes	Europe	Sub	7	(TG)₈T=0.4	delGT=0.6
1000Genomes	East Asian	Sub	4	(TG)₈T=0.8	delGT=0.2
1000Genomes	South Asian	Sub	1	(TG)₈T=0.0	delGT=1.0
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupGT=0.15

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.77991716GT[6]
GRCh38.p14 chr 13	NC_000013.11:g.77991716GT[7]
GRCh38.p14 chr 13	NC_000013.11:g.77991716GT[9]
GRCh38.p14 chr 13	NC_000013.11:g.77991716GT[10]
GRCh38.p14 chr 13	NC_000013.11:g.77991716GT[11]
GRCh37.p13 chr 13	NC_000013.10:g.78565851GT[6]
GRCh37.p13 chr 13	NC_000013.10:g.78565851GT[7]
GRCh37.p13 chr 13	NC_000013.10:g.78565851GT[9]
GRCh37.p13 chr 13	NC_000013.10:g.78565851GT[10]
GRCh37.p13 chr 13	NC_000013.10:g.78565851GT[11]

Gene: LINC01069, long intergenic non-protein coding RNA 1069 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC01069 transcript	NR_108076.1: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	(TG)₈T=	delGTGT	delGT	dupGT	dupGTGT	dup(GT)₃
GRCh38.p14 chr 13	NC_000013.11:g.77991715_77991731=	NC_000013.11:g.77991716GT[6]	NC_000013.11:g.77991716GT[7]	NC_000013.11:g.77991716GT[9]	NC_000013.11:g.77991716GT[10]	NC_000013.11:g.77991716GT[11]
GRCh37.p13 chr 13	NC_000013.10:g.78565850_78565866=	NC_000013.10:g.78565851GT[6]	NC_000013.10:g.78565851GT[7]	NC_000013.10:g.78565851GT[9]	NC_000013.10:g.78565851GT[10]	NC_000013.10:g.78565851GT[11]

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, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GMI	ss289189802	May 04, 2012 (137)
2	1000GENOMES	ss327547523	May 09, 2011 (134)
3	1000GENOMES	ss327653050	May 09, 2011 (134)
4	1000GENOMES	ss328094690	Jan 10, 2018 (151)
5	LUNTER	ss552312231	Apr 25, 2013 (138)
6	LUNTER	ss552623338	Jan 10, 2018 (151)
7	LUNTER	ss553527631	Apr 25, 2013 (138)
8	SSMP	ss664196137	Apr 01, 2015 (144)
9	1000GENOMES	ss1373390116	Jan 10, 2018 (151)
10	1000GENOMES	ss1373390120	Aug 21, 2014 (142)
11	1000GENOMES	ss1373390124	Aug 21, 2014 (142)
12	EVA_GENOME_DK	ss1574669296	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1707861515	Apr 01, 2015 (144)
14	EVA_UK10K_ALSPAC	ss1707861516	Apr 01, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1707861703	Apr 01, 2015 (144)
16	EVA_UK10K_TWINSUK	ss1707861706	Apr 01, 2015 (144)
17	SWEGEN	ss3011340061	Jan 10, 2018 (151)
18	MCHAISSO	ss3063772970	Nov 08, 2017 (151)
19	MCHAISSO	ss3064605344	Nov 08, 2017 (151)
20	EVA_DECODE	ss3695673192	Jul 13, 2019 (153)
21	EVA_DECODE	ss3695673193	Jul 13, 2019 (153)
22	EVA_DECODE	ss3695673194	Jul 13, 2019 (153)
23	EVA_DECODE	ss3695673195	Jul 13, 2019 (153)
24	ACPOP	ss3739921785	Jul 13, 2019 (153)
25	ACPOP	ss3739921786	Jul 13, 2019 (153)
26	ACPOP	ss3739921787	Jul 13, 2019 (153)
27	KHV_HUMAN_GENOMES	ss3817031718	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3817031719	Jul 13, 2019 (153)
29	KHV_HUMAN_GENOMES	ss3817031720	Jul 13, 2019 (153)
30	KHV_HUMAN_GENOMES	ss3817031721	Jul 13, 2019 (153)
31	KOGIC	ss3973924746	Apr 27, 2020 (154)
32	KOGIC	ss3973924747	Apr 27, 2020 (154)
33	GNOMAD	ss4269284387	Apr 26, 2021 (155)
34	GNOMAD	ss4269284388	Apr 26, 2021 (155)
35	GNOMAD	ss4269284389	Apr 26, 2021 (155)
36	GNOMAD	ss4269284391	Apr 26, 2021 (155)
37	GNOMAD	ss4269284392	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5210867150	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5210867151	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5210867152	Apr 26, 2021 (155)
41	1000G_HIGH_COVERAGE	ss5294403123	Oct 16, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5294403124	Oct 16, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5294403125	Oct 16, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5294403126	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5488699476	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5488699477	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5488699478	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5762982413	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5762982414	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5762982415	Oct 16, 2022 (156)
51	YY_MCH	ss5814286162	Oct 16, 2022 (156)
52	EVA	ss5839745287	Oct 16, 2022 (156)
53	EVA	ss5839745288	Oct 16, 2022 (156)
54	EVA	ss5850813137	Oct 16, 2022 (156)
55	1000Genomes	NC_000013.10 - 78565850	Oct 12, 2018 (152)
56	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 34388113 (NC_000013.10:78565849::TG 555/3854) Row 34388114 (NC_000013.10:78565849::TGTG 26/3854)	-	Oct 12, 2018 (152)
57	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 34388113 (NC_000013.10:78565849::TG 555/3854) Row 34388114 (NC_000013.10:78565849::TGTG 26/3854)	-	Oct 12, 2018 (152)
58	The Danish reference pan genome	NC_000013.10 - 78565850	Apr 27, 2020 (154)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 436427063 (NC_000013.11:77991714::TG 20811/137928) Row 436427064 (NC_000013.11:77991714::TGTG 938/138002) Row 436427065 (NC_000013.11:77991714::TGTGTG 1/138006)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 436427063 (NC_000013.11:77991714::TG 20811/137928) Row 436427064 (NC_000013.11:77991714::TGTG 938/138002) Row 436427065 (NC_000013.11:77991714::TGTGTG 1/138006)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 436427063 (NC_000013.11:77991714::TG 20811/137928) Row 436427064 (NC_000013.11:77991714::TGTG 938/138002) Row 436427065 (NC_000013.11:77991714::TGTGTG 1/138006)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 436427063 (NC_000013.11:77991714::TG 20811/137928) Row 436427064 (NC_000013.11:77991714::TGTG 938/138002) Row 436427065 (NC_000013.11:77991714::TGTGTG 1/138006)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 436427063 (NC_000013.11:77991714::TG 20811/137928) Row 436427064 (NC_000013.11:77991714::TGTG 938/138002) Row 436427065 (NC_000013.11:77991714::TGTGTG 1/138006)...	-	Apr 26, 2021 (155)
64	Korean Genome Project Submission ignored due to conflicting rows: Row 30302747 (NC_000013.11:77991714::TG 914/1832) Row 30302748 (NC_000013.11:77991714::TGTG 6/1832)	-	Apr 27, 2020 (154)
65	Korean Genome Project Submission ignored due to conflicting rows: Row 30302747 (NC_000013.11:77991714::TG 914/1832) Row 30302748 (NC_000013.11:77991714::TGTG 6/1832)	-	Apr 27, 2020 (154)
66	Northern Sweden Submission ignored due to conflicting rows: Row 13206650 (NC_000013.10:78565849::TG 93/600) Row 13206651 (NC_000013.10:78565849:TG: 8/600) Row 13206652 (NC_000013.10:78565849::TGTG 14/600)	-	Jul 13, 2019 (153)
67	Northern Sweden Submission ignored due to conflicting rows: Row 13206650 (NC_000013.10:78565849::TG 93/600) Row 13206651 (NC_000013.10:78565849:TG: 8/600) Row 13206652 (NC_000013.10:78565849::TGTG 14/600)	-	Jul 13, 2019 (153)
68	Northern Sweden Submission ignored due to conflicting rows: Row 13206650 (NC_000013.10:78565849::TG 93/600) Row 13206651 (NC_000013.10:78565849:TG: 8/600) Row 13206652 (NC_000013.10:78565849::TGTG 14/600)	-	Jul 13, 2019 (153)
69	8.3KJPN Submission ignored due to conflicting rows: Row 68836457 (NC_000013.10:78565849::TG 7927/16760) Row 68836458 (NC_000013.10:78565849::TGTG 66/16760) Row 68836459 (NC_000013.10:78565849:TG: 4/16760)	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 68836457 (NC_000013.10:78565849::TG 7927/16760) Row 68836458 (NC_000013.10:78565849::TGTG 66/16760) Row 68836459 (NC_000013.10:78565849:TG: 4/16760)	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 68836457 (NC_000013.10:78565849::TG 7927/16760) Row 68836458 (NC_000013.10:78565849::TGTG 66/16760) Row 68836459 (NC_000013.10:78565849:TG: 4/16760)	-	Apr 26, 2021 (155)
72	14KJPN Submission ignored due to conflicting rows: Row 96819517 (NC_000013.11:77991714::TG 13377/28258) Row 96819518 (NC_000013.11:77991714::TGTG 100/28258) Row 96819519 (NC_000013.11:77991714:TG: 6/28258)	-	Oct 16, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 96819517 (NC_000013.11:77991714::TG 13377/28258) Row 96819518 (NC_000013.11:77991714::TGTG 100/28258) Row 96819519 (NC_000013.11:77991714:TG: 6/28258)	-	Oct 16, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 96819517 (NC_000013.11:77991714::TG 13377/28258) Row 96819518 (NC_000013.11:77991714::TGTG 100/28258) Row 96819519 (NC_000013.11:77991714:TG: 6/28258)	-	Oct 16, 2022 (156)
75	UK 10K study - Twins Submission ignored due to conflicting rows: Row 34388113 (NC_000013.10:78565849::TG 511/3708) Row 34388114 (NC_000013.10:78565849::TGTG 29/3708)	-	Oct 12, 2018 (152)
76	UK 10K study - Twins Submission ignored due to conflicting rows: Row 34388113 (NC_000013.10:78565849::TG 511/3708) Row 34388114 (NC_000013.10:78565849::TGTG 29/3708)	-	Oct 12, 2018 (152)
77	ALFA	NC_000013.11 - 77991715	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)
rs372484049	May 15, 2013 (138)
rs372877384	May 13, 2013 (138)
rs576940987	Apr 01, 2015 (144)
rs796282547	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3695673192, ss4269284392, ss5294403126	NC_000013.11:77991714:TGTG:	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGT	(self)
12440010936	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGT	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGT	(self)
ss328094690, ss552623338	NC_000013.9:77463850:TG:	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
61889609, ss1373390116, ss3011340061, ss3739921786, ss5210867152, ss5839745288	NC_000013.10:78565849:TG:	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss3817031718, ss4269284391, ss5294403124, ss5488699477, ss5762982415	NC_000013.11:77991714:TG:	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
12440010936	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss3695673193	NC_000013.11:77991716:TG:	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss327547523, ss327653050, ss552312231, ss553527631	NC_000013.9:77463850::TG	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
ss289189802	NC_000013.9:77463867::GT	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
417739, ss664196137, ss1574669296, ss1707861515, ss1707861703, ss3739921785, ss5210867150, ss5839745287	NC_000013.10:78565849::TG	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
ss1373390120	NC_000013.10:78565851::TG	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
ss3063772970, ss3064605344, ss3817031720, ss3973924746, ss4269284387, ss5294403123, ss5488699476, ss5762982413, ss5814286162, ss5850813137	NC_000013.11:77991714::TG	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
12440010936	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
ss3817031719	NC_000013.11:77991716::TG	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
ss3695673194	NC_000013.11:77991718::TG	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
ss1707861516, ss1707861706, ss3739921787, ss5210867151	NC_000013.10:78565849::TGTG	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss1373390124	NC_000013.10:78565851::TGTG	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss3973924747, ss4269284388, ss5294403125, ss5488699478, ss5762982414	NC_000013.11:77991714::TGTG	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
12440010936	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss3817031721	NC_000013.11:77991716::TGTG	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss3695673195	NC_000013.11:77991718::TGTG	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss4269284389	NC_000013.11:77991714::TGTGTG	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
12440010936	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	NC_000013.11:77991714:TGTGTGTGTGTG… NC_000013.11:77991714:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(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 rs145357823

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

rs145357823