Name: rs3030904
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.

rs3030904

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:58330157-58330169 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: delATAT / delAT / dupAT / dupATAT
Variation Type: Indel Insertion and Deletion
Frequency: dupAT=0.11072 (1312/11850, ALFA)
dupAT=0.3357 (1681/5008, 1000G)
dupAT=0.2986 (1315/4404, Estonian) (+ 4 more)
dupAT=0.1769 (324/1832, Korea1K)
dupAT=0.338 (203/600, NorthernSweden)
dupAT=0.324 (70/216, Vietnamese)
dupAT=0.28 (11/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TSPOAP1-AS1 : Intron Variant
TSPOAP1 : 2KB Upstream 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	11850	TATATATATATAT=0.88599	TATATATAT=0.00000, TATATATATAT=0.00329, TATATATATATATAT=0.11072, TATATATATATATATAT=0.00000	0.813626	0.034149	0.152226	32
European	Sub	10092	TATATATATATAT=0.86643	TATATATAT=0.00000, TATATATATAT=0.00386, TATATATATATATAT=0.12971, TATATATATATATATAT=0.00000	0.781506	0.040144	0.17835	32
African	Sub	930	TATATATATATAT=1.000	TATATATAT=0.000, TATATATATAT=0.000, TATATATATATATAT=0.000, TATATATATATATATAT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	32	TATATATATATAT=1.00	TATATATAT=0.00, TATATATATAT=0.00, TATATATATATATAT=0.00, TATATATATATATATAT=0.00	1.0	0.0	0.0	N/A
African American	Sub	898	TATATATATATAT=1.000	TATATATAT=0.000, TATATATATAT=0.000, TATATATATATATAT=0.000, TATATATATATATATAT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	64	TATATATATATAT=1.00	TATATATAT=0.00, TATATATATAT=0.00, TATATATATATATAT=0.00, TATATATATATATATAT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	50	TATATATATATAT=1.00	TATATATAT=0.00, TATATATATAT=0.00, TATATATATATATAT=0.00, TATATATATATATATAT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	14	TATATATATATAT=1.00	TATATATAT=0.00, TATATATATAT=0.00, TATATATATATATAT=0.00, TATATATATATATATAT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	82	TATATATATATAT=1.00	TATATATAT=0.00, TATATATATAT=0.00, TATATATATATATAT=0.00, TATATATATATATATAT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	388	TATATATATATAT=1.000	TATATATAT=0.000, TATATATATAT=0.000, TATATATATATATAT=0.000, TATATATATATATATAT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	42	TATATATATATAT=1.00	TATATATAT=0.00, TATATATATAT=0.00, TATATATATATATAT=0.00, TATATATATATATATAT=0.00	1.0	0.0	0.0	N/A
Other	Sub	252	TATATATATATAT=0.988	TATATATAT=0.000, TATATATATAT=0.000, TATATATATATATAT=0.012, TATATATATATATATAT=0.000	0.97619	0.0	0.02381	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	11850	(TA)₆T=0.88599	delATAT=0.00000, delAT=0.00329, dupAT=0.11072, dupATAT=0.00000
Allele Frequency Aggregator	European	Sub	10092	(TA)₆T=0.86643	delATAT=0.00000, delAT=0.00386, dupAT=0.12971, dupATAT=0.00000
Allele Frequency Aggregator	African	Sub	930	(TA)₆T=1.000	delATAT=0.000, delAT=0.000, dupAT=0.000, dupATAT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	388	(TA)₆T=1.000	delATAT=0.000, delAT=0.000, dupAT=0.000, dupATAT=0.000
Allele Frequency Aggregator	Other	Sub	252	(TA)₆T=0.988	delATAT=0.000, delAT=0.000, dupAT=0.012, dupATAT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	82	(TA)₆T=1.00	delATAT=0.00, delAT=0.00, dupAT=0.00, dupATAT=0.00
Allele Frequency Aggregator	Asian	Sub	64	(TA)₆T=1.00	delATAT=0.00, delAT=0.00, dupAT=0.00, dupATAT=0.00
Allele Frequency Aggregator	South Asian	Sub	42	(TA)₆T=1.00	delATAT=0.00, delAT=0.00, dupAT=0.00, dupATAT=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupAT=0.3357
1000Genomes	African	Sub	1322	- No frequency provided	dupAT=0.4992
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupAT=0.2292
1000Genomes	Europe	Sub	1006	- No frequency provided	dupAT=0.3062
1000Genomes	South Asian	Sub	978	- No frequency provided	dupAT=0.351
1000Genomes	American	Sub	694	- No frequency provided	dupAT=0.200
Genetic variation in the Estonian population	Estonian	Study-wide	4404	- No frequency provided	dupAT=0.2986
Korean Genome Project	KOREAN	Study-wide	1832	- No frequency provided	dupAT=0.1769
Northern Sweden	ACPOP	Study-wide	600	- No frequency provided	dupAT=0.338
A Vietnamese Genetic Variation Database	Global	Study-wide	216	- No frequency provided	dupAT=0.324
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupAT=0.28

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 17	NC_000017.11:g.58330158AT[4]
GRCh38.p14 chr 17	NC_000017.11:g.58330158AT[5]
GRCh38.p14 chr 17	NC_000017.11:g.58330158AT[7]
GRCh38.p14 chr 17	NC_000017.11:g.58330158AT[8]
GRCh37.p13 chr 17	NC_000017.10:g.56407519AT[4]
GRCh37.p13 chr 17	NC_000017.10:g.56407519AT[5]
GRCh37.p13 chr 17	NC_000017.10:g.56407519AT[7]
GRCh37.p13 chr 17	NC_000017.10:g.56407519AT[8]

Gene: TSPOAP1, TSPO associated protein 1 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
TSPOAP1 transcript variant 3	NM_001261835.2:c.	N/A	Upstream Transcript Variant
TSPOAP1 transcript variant 1	NM_004758.4:c.	N/A	Upstream Transcript Variant
TSPOAP1 transcript variant 2	NM_024418.3:c.	N/A	Upstream Transcript Variant

Gene: TSPOAP1-AS1, TSPOAP1, SUPT4H1 and RNF43 antisense RNA 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TSPOAP1-AS1 transcript variant 1	NR_038410.1:n.	N/A	Intron Variant
TSPOAP1-AS1 transcript variant 2	NR_038411.1:n.	N/A	Intron Variant
TSPOAP1-AS1 transcript variant 3	NR_038412.1:n.	N/A	Intron Variant
TSPOAP1-AS1 transcript variant 4	NR_038413.1:n.	N/A	Intron Variant
TSPOAP1-AS1 transcript variant 5	NR_038414.1:n.	N/A	Genic Upstream Transcript Variant
TSPOAP1-AS1 transcript variant 6	NR_038415.1:n.	N/A	Genic Upstream Transcript Variant
TSPOAP1-AS1 transcript variant 7	NR_038416.1:n.	N/A	Genic Upstream Transcript Variant
TSPOAP1-AS1 transcript variant 8	NR_038417.1:n.	N/A	Genic Upstream Transcript Variant
TSPOAP1-AS1 transcript variant 9	NR_038418.1:n.	N/A	Genic Upstream 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	(TA)₆T=	delATAT	delAT	dupAT	dupATAT
GRCh38.p14 chr 17	NC_000017.11:g.58330157_58330169=	NC_000017.11:g.58330158AT[4]	NC_000017.11:g.58330158AT[5]	NC_000017.11:g.58330158AT[7]	NC_000017.11:g.58330158AT[8]
GRCh37.p13 chr 17	NC_000017.10:g.56407518_56407530=	NC_000017.10:g.56407519AT[4]	NC_000017.10:g.56407519AT[5]	NC_000017.10:g.56407519AT[7]	NC_000017.10:g.56407519AT[8]

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#.

55 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss4261940	Dec 03, 2013 (138)
2	ABI	ss40777125	Dec 03, 2013 (138)
3	HGSV	ss82136086	Dec 04, 2013 (138)
4	HGSV	ss82804346	Dec 05, 2013 (138)
5	HGSV	ss82878180	Dec 05, 2013 (138)
6	HUMANGENOME_JCVI	ss95697462	Dec 05, 2013 (138)
7	GMI	ss289331858	May 04, 2012 (137)
8	1000GENOMES	ss327796659	May 09, 2011 (135)
9	1000GENOMES	ss327923031	May 09, 2011 (135)
10	1000GENOMES	ss328225051	May 09, 2011 (135)
11	LUNTER	ss552533768	Apr 25, 2013 (138)
12	LUNTER	ss552887315	Apr 25, 2013 (138)
13	LUNTER	ss553622492	Apr 25, 2013 (138)
14	SSMP	ss664366382	Apr 01, 2015 (144)
15	1000GENOMES	ss1376786072	Aug 21, 2014 (142)
16	DDI	ss1536851370	Apr 01, 2015 (144)
17	EVA_GENOME_DK	ss1575067196	Apr 01, 2015 (144)
18	EVA_UK10K_ALSPAC	ss1708801364	Jan 10, 2018 (151)
19	EVA_UK10K_TWINSUK	ss1708801411	Jan 10, 2018 (151)
20	EVA_UK10K_TWINSUK	ss1710737231	Apr 01, 2015 (144)
21	EVA_UK10K_ALSPAC	ss1710737232	Apr 01, 2015 (144)
22	HAMMER_LAB	ss1808829016	Sep 08, 2015 (146)
23	JJLAB	ss2031342905	Sep 14, 2016 (149)
24	SWEGEN	ss3015712686	Jan 10, 2018 (151)
25	MCHAISSO	ss3064715973	Nov 08, 2017 (151)
26	MCHAISSO	ss3065656155	Nov 08, 2017 (151)
27	BEROUKHIMLAB	ss3644414363	Oct 12, 2018 (152)
28	BIOINF_KMB_FNS_UNIBA	ss3645459475	Oct 12, 2018 (152)
29	URBANLAB	ss3650678432	Oct 12, 2018 (152)
30	EGCUT_WGS	ss3682590539	Jul 13, 2019 (153)
31	EVA_DECODE	ss3700681381	Jul 13, 2019 (153)
32	EVA_DECODE	ss3700681382	Jul 13, 2019 (153)
33	ACPOP	ss3742118310	Jul 13, 2019 (153)
34	KHV_HUMAN_GENOMES	ss3820060617	Jul 13, 2019 (153)
35	EVA	ss3834921154	Apr 27, 2020 (154)
36	EVA	ss3841073468	Apr 27, 2020 (154)
37	EVA	ss3846570763	Apr 27, 2020 (154)
38	KOGIC	ss3979051698	Apr 27, 2020 (154)
39	GNOMAD	ss4313512819	Apr 26, 2021 (155)
40	GNOMAD	ss4313512820	Apr 26, 2021 (155)
41	GNOMAD	ss4313512821	Apr 26, 2021 (155)
42	GNOMAD	ss4313512822	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5222923042	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5222923043	Apr 26, 2021 (155)
45	1000G_HIGH_COVERAGE	ss5303511522	Oct 16, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5303511523	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5496521165	Oct 16, 2022 (156)
48	EVA	ss5511798092	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5779288680	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5779288681	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5779288682	Oct 16, 2022 (156)
52	YY_MCH	ss5816629855	Oct 16, 2022 (156)
53	EVA	ss5834129837	Oct 16, 2022 (156)
54	EVA	ss5834129838	Oct 16, 2022 (156)
55	EVA	ss5851849302	Oct 16, 2022 (156)
56	1000Genomes	NC_000017.10 - 56407518	Oct 12, 2018 (152)
57	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 40086827 (NC_000017.10:56407517::TA 1170/3854) Row 40086828 (NC_000017.10:56407517:TA: 61/3854)	-	Oct 12, 2018 (152)
58	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 40086827 (NC_000017.10:56407517::TA 1170/3854) Row 40086828 (NC_000017.10:56407517:TA: 61/3854)	-	Oct 12, 2018 (152)
59	Genetic variation in the Estonian population	NC_000017.10 - 56407518	Oct 12, 2018 (152)
60	The Danish reference pan genome	NC_000017.10 - 56407518	Apr 27, 2020 (154)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510409113 (NC_000017.11:58330156::TA 47908/139526) Row 510409114 (NC_000017.11:58330156::TATA 19/139602) Row 510409115 (NC_000017.11:58330156:TA: 204/139598)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510409113 (NC_000017.11:58330156::TA 47908/139526) Row 510409114 (NC_000017.11:58330156::TATA 19/139602) Row 510409115 (NC_000017.11:58330156:TA: 204/139598)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510409113 (NC_000017.11:58330156::TA 47908/139526) Row 510409114 (NC_000017.11:58330156::TATA 19/139602) Row 510409115 (NC_000017.11:58330156:TA: 204/139598)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510409113 (NC_000017.11:58330156::TA 47908/139526) Row 510409114 (NC_000017.11:58330156::TATA 19/139602) Row 510409115 (NC_000017.11:58330156:TA: 204/139598)...	-	Apr 26, 2021 (155)
65	Korean Genome Project	NC_000017.11 - 58330157	Apr 27, 2020 (154)
66	Northern Sweden	NC_000017.10 - 56407518	Jul 13, 2019 (153)
67	8.3KJPN Submission ignored due to conflicting rows: Row 80892349 (NC_000017.10:56407517::TA 3390/16758) Row 80892350 (NC_000017.10:56407517:TA: 1/16758)	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 80892349 (NC_000017.10:56407517::TA 3390/16758) Row 80892350 (NC_000017.10:56407517:TA: 1/16758)	-	Apr 26, 2021 (155)
69	14KJPN Submission ignored due to conflicting rows: Row 113125784 (NC_000017.11:58330156::TA 5676/28258) Row 113125785 (NC_000017.11:58330156:TA: 1/28258) Row 113125786 (NC_000017.11:58330156::TATA 1/28258)	-	Oct 16, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 113125784 (NC_000017.11:58330156::TA 5676/28258) Row 113125785 (NC_000017.11:58330156:TA: 1/28258) Row 113125786 (NC_000017.11:58330156::TATA 1/28258)	-	Oct 16, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 113125784 (NC_000017.11:58330156::TA 5676/28258) Row 113125785 (NC_000017.11:58330156:TA: 1/28258) Row 113125786 (NC_000017.11:58330156::TATA 1/28258)	-	Oct 16, 2022 (156)
72	UK 10K study - Twins Submission ignored due to conflicting rows: Row 40086827 (NC_000017.10:56407517::TA 1116/3708) Row 40086828 (NC_000017.10:56407517:TA: 55/3708)	-	Oct 12, 2018 (152)
73	UK 10K study - Twins Submission ignored due to conflicting rows: Row 40086827 (NC_000017.10:56407517::TA 1116/3708) Row 40086828 (NC_000017.10:56407517:TA: 55/3708)	-	Oct 12, 2018 (152)
74	A Vietnamese Genetic Variation Database	NC_000017.10 - 56407518	Jul 13, 2019 (153)
75	ALFA	NC_000017.11 - 58330157	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)
rs34490087	May 15, 2013 (138)
rs60154711	May 26, 2008 (130)
rs71829385	May 11, 2012 (137)
rs72410834	May 11, 2012 (137)
rs142026054	Sep 17, 2011 (135)
rs796775300	Nov 08, 2017 (151)
rs146268942	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4313512822	NC_000017.11:58330156:TATA:	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATAT	(self)
12787707377	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATAT	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATAT	(self)
ss1708801364, ss1708801411, ss3015712686, ss5222923043, ss5511798092, ss5834129838	NC_000017.10:56407517:TA:	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATATAT	(self)
ss3700681381, ss4313512821, ss5303511523, ss5779288681	NC_000017.11:58330156:TA:	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATATAT	(self)
12787707377	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATATAT	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATATAT	(self)
ss327796659, ss327923031, ss328225051, ss552533768, ss552887315, ss553622492	NC_000017.9:53762516::TA	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATATATATAT	(self)
ss289331858	NC_000017.9:53762529::AT	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATATATATAT	(self)
72336184, 28328787, 568533, 15403175, 8866285, ss664366382, ss1376786072, ss1536851370, ss1575067196, ss1808829016, ss2031342905, ss3644414363, ss3682590539, ss3742118310, ss3834921154, ss3841073468, ss5222923042, ss5834129837	NC_000017.10:56407517::TA	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATATATATAT	(self)
ss1710737231, ss1710737232	NC_000017.10:56407519::TA	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATATATATAT	(self)
35429699, ss3064715973, ss3065656155, ss3645459475, ss3650678432, ss3820060617, ss3846570763, ss3979051698, ss4313512819, ss5303511522, ss5496521165, ss5779288680, ss5816629855, ss5851849302	NC_000017.11:58330156::TA	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATATATATAT	(self)
12787707377	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATATATATAT	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATATATATAT	(self)
ss3700681382	NC_000017.11:58330158::TA	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATATATATAT	(self)
ss4261940, ss40777125, ss82136086, ss82804346, ss82878180, ss95697462	NT_010783.15:21681682::AT	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATATATATAT	(self)
ss4313512820, ss5779288682	NC_000017.11:58330156::TATA	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATATATATATAT	(self)
12787707377	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATATATATATAT	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATATATATATAT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2382866646	NC_000017.10:56407517:TATA:	NC_000017.11:58330156:TATATATATATA… NC_000017.11:58330156:TATATATATATAT:TATATATAT

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs3030904

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

rs3030904