Name: rs61128042
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.

rs61128042

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:80999046-80999054 (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)₄ / delTT / delT / dupT / du…
del(T)₄ / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₆ / ins(T)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: dupTT=0.02494 (352/14116, ALFA)
dupTT=0.1382 (692/5008, 1000G)
dupTT=0.2 (2/8, KOREAN)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MIR4514 : 2KB Upstream Variant
TLNRD1 : 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	14116	TTTTTTTTT=0.95863	TTTTT=0.00000, TTTTTTT=0.00000, TTTTTTTT=0.00000, TTTTTTTTTT=0.01644, TTTTTTTTTTT=0.02494, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000	0.95403	0.001768	0.044202	10
European	Sub	11287	TTTTTTTTT=0.94826	TTTTT=0.00000, TTTTTTT=0.00000, TTTTTTTT=0.00000, TTTTTTTTTT=0.02055, TTTTTTTTTTT=0.03119, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000	0.941932	0.002233	0.055835	7
African	Sub	1730	TTTTTTTTT=1.0000	TTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	72	TTTTTTTTT=1.00	TTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1658	TTTTTTTTT=1.0000	TTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	94	TTTTTTTTT=1.00	TTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	70	TTTTTTTTT=1.00	TTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	24	TTTTTTTTT=1.00	TTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	98	TTTTTTTTT=1.00	TTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	448	TTTTTTTTT=1.000	TTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	80	TTTTTTTTT=1.00	TTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	379	TTTTTTTTT=1.000	TTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=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	14116	(T)₉=0.95863	del(T)₄=0.00000, delTT=0.00000, delT=0.00000, dupT=0.01644, dupTT=0.02494, dupTTT=0.00000, dup(T)₄=0.00000
Allele Frequency Aggregator	European	Sub	11287	(T)₉=0.94826	del(T)₄=0.00000, delTT=0.00000, delT=0.00000, dupT=0.02055, dupTT=0.03119, dupTTT=0.00000, dup(T)₄=0.00000
Allele Frequency Aggregator	African	Sub	1730	(T)₉=1.0000	del(T)₄=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	448	(T)₉=1.000	del(T)₄=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	379	(T)₉=1.000	del(T)₄=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	98	(T)₉=1.00	del(T)₄=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	94	(T)₉=1.00	del(T)₄=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	80	(T)₉=1.00	del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupTT=0.1382
1000Genomes	African	Sub	1322	- No frequency provided	dupTT=0.1815
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupTT=0.1369
1000Genomes	Europe	Sub	1006	- No frequency provided	dupTT=0.1292
1000Genomes	South Asian	Sub	978	- No frequency provided	dupTT=0.096
1000Genomes	American	Sub	694	- No frequency provided	dupTT=0.130
KOREAN population from KRGDB	KOREAN	Study-wide	8	- No frequency provided	dupTT=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 15	NC_000015.10:g.80999051_80999054del
GRCh38.p14 chr 15	NC_000015.10:g.80999053_80999054del
GRCh38.p14 chr 15	NC_000015.10:g.80999054del
GRCh38.p14 chr 15	NC_000015.10:g.80999054dup
GRCh38.p14 chr 15	NC_000015.10:g.80999053_80999054dup
GRCh38.p14 chr 15	NC_000015.10:g.80999052_80999054dup
GRCh38.p14 chr 15	NC_000015.10:g.80999051_80999054dup
GRCh38.p14 chr 15	NC_000015.10:g.80999049_80999054dup
GRCh38.p14 chr 15	NC_000015.10:g.80999054_80999055insTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.81291392_81291395del
GRCh37.p13 chr 15	NC_000015.9:g.81291394_81291395del
GRCh37.p13 chr 15	NC_000015.9:g.81291395del
GRCh37.p13 chr 15	NC_000015.9:g.81291395dup
GRCh37.p13 chr 15	NC_000015.9:g.81291394_81291395dup
GRCh37.p13 chr 15	NC_000015.9:g.81291393_81291395dup
GRCh37.p13 chr 15	NC_000015.9:g.81291392_81291395dup
GRCh37.p13 chr 15	NC_000015.9:g.81291390_81291395dup
GRCh37.p13 chr 15	NC_000015.9:g.81291395_81291396insTTTTTTTTTT
TLNRD1 RefSeqGene	NG_052069.1:g.3098_3101del
TLNRD1 RefSeqGene	NG_052069.1:g.3100_3101del
TLNRD1 RefSeqGene	NG_052069.1:g.3101del
TLNRD1 RefSeqGene	NG_052069.1:g.3101dup
TLNRD1 RefSeqGene	NG_052069.1:g.3100_3101dup
TLNRD1 RefSeqGene	NG_052069.1:g.3099_3101dup
TLNRD1 RefSeqGene	NG_052069.1:g.3098_3101dup
TLNRD1 RefSeqGene	NG_052069.1:g.3096_3101dup
TLNRD1 RefSeqGene	NG_052069.1:g.3101_3102insTTTTTTTTTT

Gene: TLNRD1, talin rod domain containing 1 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
TLNRD1 transcript	NM_022566.3:c.	N/A	Upstream Transcript Variant

Gene: MIR4514, microRNA 4514 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
MIR4514 transcript	NR_039739.1:n.	N/A	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	(T)₉=	del(T)₄	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₆	ins(T)₁₀
GRCh38.p14 chr 15	NC_000015.10:g.80999046_80999054=	NC_000015.10:g.80999051_80999054del	NC_000015.10:g.80999053_80999054del	NC_000015.10:g.80999054del	NC_000015.10:g.80999054dup	NC_000015.10:g.80999053_80999054dup	NC_000015.10:g.80999052_80999054dup	NC_000015.10:g.80999051_80999054dup	NC_000015.10:g.80999049_80999054dup	NC_000015.10:g.80999054_80999055insTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.81291387_81291395=	NC_000015.9:g.81291392_81291395del	NC_000015.9:g.81291394_81291395del	NC_000015.9:g.81291395del	NC_000015.9:g.81291395dup	NC_000015.9:g.81291394_81291395dup	NC_000015.9:g.81291393_81291395dup	NC_000015.9:g.81291392_81291395dup	NC_000015.9:g.81291390_81291395dup	NC_000015.9:g.81291395_81291396insTTTTTTTTTT
TLNRD1 RefSeqGene	NG_052069.1:g.3093_3101=	NG_052069.1:g.3098_3101del	NG_052069.1:g.3100_3101del	NG_052069.1:g.3101del	NG_052069.1:g.3101dup	NG_052069.1:g.3100_3101dup	NG_052069.1:g.3099_3101dup	NG_052069.1:g.3098_3101dup	NG_052069.1:g.3096_3101dup	NG_052069.1:g.3101_3102insTTTTTTTTTT

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#.

46 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80199704	Dec 16, 2007 (129)
2	LUNTER	ss552435140	Apr 25, 2013 (138)
3	LUNTER	ss552763366	Apr 25, 2013 (138)
4	LUNTER	ss553581273	Apr 25, 2013 (138)
5	SSMP	ss664289427	Apr 01, 2015 (144)
6	BILGI_BIOE	ss666655933	Apr 25, 2013 (138)
7	SSIP	ss947346968	Aug 21, 2014 (142)
8	1000GENOMES	ss1375176026	Aug 21, 2014 (142)
9	SWEGEN	ss3013624273	Nov 08, 2017 (151)
10	SWEGEN	ss3013624274	Nov 08, 2017 (151)
11	MCHAISSO	ss3063827051	Nov 08, 2017 (151)
12	EVA_DECODE	ss3698306131	Jul 13, 2019 (153)
13	EVA_DECODE	ss3698306132	Jul 13, 2019 (153)
14	EVA_DECODE	ss3698306133	Jul 13, 2019 (153)
15	EVA_DECODE	ss3698306134	Jul 13, 2019 (153)
16	EVA_DECODE	ss3698306135	Jul 13, 2019 (153)
17	EVA_DECODE	ss3698306136	Jul 13, 2019 (153)
18	ACPOP	ss3741103887	Jul 13, 2019 (153)
19	ACPOP	ss3741103888	Jul 13, 2019 (153)
20	PACBIO	ss3787906813	Jul 13, 2019 (153)
21	PACBIO	ss3792909115	Jul 13, 2019 (153)
22	PACBIO	ss3792909116	Jul 13, 2019 (153)
23	PACBIO	ss3797793706	Jul 13, 2019 (153)
24	KHV_HUMAN_GENOMES	ss3818652941	Jul 13, 2019 (153)
25	EVA	ss3834339201	Apr 27, 2020 (154)
26	KRGDB	ss3932586496	Apr 27, 2020 (154)
27	KOGIC	ss3976580384	Apr 27, 2020 (154)
28	KOGIC	ss3976580385	Apr 27, 2020 (154)
29	KOGIC	ss3976580387	Apr 27, 2020 (154)
30	GNOMAD	ss4292438507	Apr 26, 2021 (155)
31	GNOMAD	ss4292438508	Apr 26, 2021 (155)
32	GNOMAD	ss4292438509	Apr 26, 2021 (155)
33	GNOMAD	ss4292438512	Apr 26, 2021 (155)
34	GNOMAD	ss4292438513	Apr 26, 2021 (155)
35	TOPMED	ss4998755453	Apr 26, 2021 (155)
36	TOPMED	ss4998755455	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5217177158	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5217177159	Apr 26, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5299177662	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5492828062	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5492828064	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5771277216	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5771277217	Oct 16, 2022 (156)
44	EVA	ss5828487029	Oct 16, 2022 (156)
45	EVA	ss5828487030	Oct 16, 2022 (156)
46	EVA	ss5851379525	Oct 16, 2022 (156)
47	1000Genomes	NC_000015.9 - 81291387	Oct 12, 2018 (152)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 475206533 (NC_000015.10:80999045::T 8508/138362) Row 475206534 (NC_000015.10:80999045::TT 17513/138324) Row 475206535 (NC_000015.10:80999045::TTT 12/138410)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 475206533 (NC_000015.10:80999045::T 8508/138362) Row 475206534 (NC_000015.10:80999045::TT 17513/138324) Row 475206535 (NC_000015.10:80999045::TTT 12/138410)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 475206533 (NC_000015.10:80999045::T 8508/138362) Row 475206534 (NC_000015.10:80999045::TT 17513/138324) Row 475206535 (NC_000015.10:80999045::TTT 12/138410)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 475206533 (NC_000015.10:80999045::T 8508/138362) Row 475206534 (NC_000015.10:80999045::TT 17513/138324) Row 475206535 (NC_000015.10:80999045::TTT 12/138410)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 475206533 (NC_000015.10:80999045::T 8508/138362) Row 475206534 (NC_000015.10:80999045::TT 17513/138324) Row 475206535 (NC_000015.10:80999045::TTT 12/138410)...	-	Apr 26, 2021 (155)
53	KOREAN population from KRGDB	NC_000015.9 - 81291387	Apr 27, 2020 (154)
54	Korean Genome Project Submission ignored due to conflicting rows: Row 32958385 (NC_000015.10:80999045::TT 278/1828) Row 32958386 (NC_000015.10:80999045::T 21/1828) Row 32958388 (NC_000015.10:80999045::TTT 2/1828)	-	Apr 27, 2020 (154)
55	Korean Genome Project Submission ignored due to conflicting rows: Row 32958385 (NC_000015.10:80999045::TT 278/1828) Row 32958386 (NC_000015.10:80999045::T 21/1828) Row 32958388 (NC_000015.10:80999045::TTT 2/1828)	-	Apr 27, 2020 (154)
56	Korean Genome Project Submission ignored due to conflicting rows: Row 32958385 (NC_000015.10:80999045::TT 278/1828) Row 32958386 (NC_000015.10:80999045::T 21/1828) Row 32958388 (NC_000015.10:80999045::TTT 2/1828)	-	Apr 27, 2020 (154)
57	Northern Sweden Submission ignored due to conflicting rows: Row 14388752 (NC_000015.9:81291386::TT 39/598) Row 14388753 (NC_000015.9:81291386::T 22/598)	-	Jul 13, 2019 (153)
58	Northern Sweden Submission ignored due to conflicting rows: Row 14388752 (NC_000015.9:81291386::TT 39/598) Row 14388753 (NC_000015.9:81291386::T 22/598)	-	Jul 13, 2019 (153)
59	8.3KJPN Submission ignored due to conflicting rows: Row 75146465 (NC_000015.9:81291386::TT 2377/16758) Row 75146466 (NC_000015.9:81291386::T 90/16758)	-	Apr 26, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 75146465 (NC_000015.9:81291386::TT 2377/16758) Row 75146466 (NC_000015.9:81291386::T 90/16758)	-	Apr 26, 2021 (155)
61	14KJPN Submission ignored due to conflicting rows: Row 105114320 (NC_000015.10:80999045::T 174/28258) Row 105114321 (NC_000015.10:80999045::TT 4013/28258)	-	Oct 16, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 105114320 (NC_000015.10:80999045::T 174/28258) Row 105114321 (NC_000015.10:80999045::TT 4013/28258)	-	Oct 16, 2022 (156)
63	TopMed Submission ignored due to conflicting rows: Row 214301113 (NC_000015.10:80999045::T 16452/264690) Row 214301115 (NC_000015.10:80999045:TTTT: 1/264690)	-	Apr 26, 2021 (155)
64	TopMed Submission ignored due to conflicting rows: Row 214301113 (NC_000015.10:80999045::T 16452/264690) Row 214301115 (NC_000015.10:80999045:TTTT: 1/264690)	-	Apr 26, 2021 (155)
65	ALFA	NC_000015.10 - 80999046	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4998755455	NC_000015.10:80999045:TTTT:	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTT	(self)
8516685973	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTT	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTT	(self)
8516685973	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTT	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTT	(self)
ss4292438513	NC_000015.10:80999045:T:	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTT	(self)
8516685973	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTT	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTT	(self)
ss666655933, ss3013624273, ss3741103888, ss3792909115, ss5217177159, ss5828487030	NC_000015.9:81291386::T	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTT	(self)
ss3698306131, ss3976580385, ss4292438507, ss4998755453, ss5492828062, ss5771277216	NC_000015.10:80999045::T	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTT	(self)
8516685973	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTT	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTT	(self)
ss552435140, ss552763366, ss553581273	NC_000015.8:79078441::TT	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTTT	(self)
67405895, 39763890, ss664289427, ss947346968, ss1375176026, ss3013624274, ss3741103887, ss3787906813, ss3792909116, ss3797793706, ss3834339201, ss3932586496, ss5217177158, ss5828487029	NC_000015.9:81291386::TT	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTTT	(self)
ss3063827051, ss3698306132, ss3818652941, ss3976580384, ss4292438508, ss5299177662, ss5492828064, ss5771277217, ss5851379525	NC_000015.10:80999045::TT	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTTT	(self)
8516685973	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTTT	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTTT	(self)
ss80199704	NT_010194.17:52081952::TT	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTTT	(self)
ss3698306133, ss3976580387, ss4292438509	NC_000015.10:80999045::TTT	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTTTT	(self)
8516685973	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTTTT	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTTTT	(self)
ss3698306134, ss4292438512	NC_000015.10:80999045::TTTT	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTTTTT	(self)
8516685973	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTTTTT	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3698306135	NC_000015.10:80999045::TTTTTT	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3698306136	NC_000015.10:80999045::TTTTTTTTTT	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2372996245	NC_000015.9:81291386:TTTT:	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTT
ss3233158119	NC_000015.10:80999045:TT:	NC_000015.10:80999045:TTTTTTTTT:TT… NC_000015.10:80999045:TTTTTTTTT:TTTTTTT

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

No publications for rs61128042

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

rs61128042