Name: rs55730814
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.

rs55730814

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:74834861-74834905 (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: delC(TGA)₂TTCACATTCTC / dupC(TGA)₂…
delC(TGA)₂TTCACATTCTC / dupC(TGA)₂TTCACATTCTC
Variation Type: Indel Insertion and Deletion
Frequency: delC(TGA)₂TTCACATTCTC=0.425853 (112719/264690, TOPMED)
delC(TGA)₂TTCACATTCTC=0.03305 (934/28258, 14KJPN)
delC(TGA)₂TTCACATTCTC=0.03234 (542/16760, 8.3KJPN) (+ 9 more)
delC(TGA)₂TTCACATTCTC=0.26968 (2823/10468, ALFA)
delC(TGA)₂TTCACATTCTC=0.3584 (2295/6404, 1000G_30x)
delC(TGA)₂TTCACATTCTC=0.3273 (1639/5008, 1000G)
delC(TGA)₂TTCACATTCTC=0.4089 (1576/3854, ALSPAC)
delC(TGA)₂TTCACATTCTC=0.3964 (1470/3708, TWINSUK)
delC(TGA)₂TTCACATTCTC=0.0442 (81/1832, Korea1K)
delC(TGA)₂TTCACATTCTC=0.391 (390/998, GoNL)
delC(TGA)₂TTCACATTCTC=0.372 (223/600, NorthernSweden)
delC(TGA)₂TTCACATTCTC=0.15 (6/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PI15 : 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	10468	CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.73032	CACATTCTCCTGATGATTCACATTCTC=0.26968, CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.00000	0.569927	0.109285	0.320787	32
European	Sub	9132	CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.6984	CACATTCTCCTGATGATTCACATTCTC=0.3016, CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.0000	0.517302	0.120456	0.362243	32
African	Sub	586	CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.915	CACATTCTCCTGATGATTCACATTCTC=0.085, CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.000	0.887372	0.05802	0.054608	32
African Others	Sub	26	CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.96	CACATTCTCCTGATGATTCACATTCTC=0.04, CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.00	0.923077	0.0	0.076923	0
African American	Sub	560	CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.912	CACATTCTCCTGATGATTCACATTCTC=0.087, CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.000	0.885714	0.060714	0.053571	32
Asian	Sub	102	CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=1.000	CACATTCTCCTGATGATTCACATTCTC=0.000, CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.000	1.0	0.0	0.0	N/A
East Asian	Sub	80	CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=1.00	CACATTCTCCTGATGATTCACATTCTC=0.00, CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	22	CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=1.00	CACATTCTCCTGATGATTCACATTCTC=0.00, CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	46	CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=1.00	CACATTCTCCTGATGATTCACATTCTC=0.00, CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	358	CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=1.000	CACATTCTCCTGATGATTCACATTCTC=0.000, CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	36	CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.97	CACATTCTCCTGATGATTCACATTCTC=0.03, CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.00	0.944444	0.0	0.055556	0
Other	Sub	208	CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.913	CACATTCTCCTGATGATTCACATTCTC=0.087, CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC=0.000	0.875	0.048077	0.076923	15

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
TopMed	Global	Study-wide	264690	(CACATTCTCCTGATGATT)₂CACATTCTC=0.574147	delC(TGA)₂TTCACATTCTC=0.425853
14KJPN	JAPANESE	Study-wide	28258	(CACATTCTCCTGATGATT)₂CACATTCTC=0.96695	delC(TGA)₂TTCACATTCTC=0.03305
8.3KJPN	JAPANESE	Study-wide	16760	(CACATTCTCCTGATGATT)₂CACATTCTC=0.96766	delC(TGA)₂TTCACATTCTC=0.03234
Allele Frequency Aggregator	Total	Global	10468	(CACATTCTCCTGATGATT)₂CACATTCTC=0.73032	delC(TGA)₂TTCACATTCTC=0.26968, dupC(TGA)₂TTCACATTCTC=0.00000
Allele Frequency Aggregator	European	Sub	9132	(CACATTCTCCTGATGATT)₂CACATTCTC=0.6984	delC(TGA)₂TTCACATTCTC=0.3016, dupC(TGA)₂TTCACATTCTC=0.0000
Allele Frequency Aggregator	African	Sub	586	(CACATTCTCCTGATGATT)₂CACATTCTC=0.915	delC(TGA)₂TTCACATTCTC=0.085, dupC(TGA)₂TTCACATTCTC=0.000
Allele Frequency Aggregator	Latin American 2	Sub	358	(CACATTCTCCTGATGATT)₂CACATTCTC=1.000	delC(TGA)₂TTCACATTCTC=0.000, dupC(TGA)₂TTCACATTCTC=0.000
Allele Frequency Aggregator	Other	Sub	208	(CACATTCTCCTGATGATT)₂CACATTCTC=0.913	delC(TGA)₂TTCACATTCTC=0.087, dupC(TGA)₂TTCACATTCTC=0.000
Allele Frequency Aggregator	Asian	Sub	102	(CACATTCTCCTGATGATT)₂CACATTCTC=1.000	delC(TGA)₂TTCACATTCTC=0.000, dupC(TGA)₂TTCACATTCTC=0.000
Allele Frequency Aggregator	Latin American 1	Sub	46	(CACATTCTCCTGATGATT)₂CACATTCTC=1.00	delC(TGA)₂TTCACATTCTC=0.00, dupC(TGA)₂TTCACATTCTC=0.00
Allele Frequency Aggregator	South Asian	Sub	36	(CACATTCTCCTGATGATT)₂CACATTCTC=0.97	delC(TGA)₂TTCACATTCTC=0.03, dupC(TGA)₂TTCACATTCTC=0.00
1000Genomes_30x	Global	Study-wide	6404	(CACATTCTCCTGATGATT)₂CACATTCTC=0.6416	delC(TGA)₂TTCACATTCTC=0.3584
1000Genomes_30x	African	Sub	1786	(CACATTCTCCTGATGATT)₂CACATTCTC=0.4406	delC(TGA)₂TTCACATTCTC=0.5594
1000Genomes_30x	Europe	Sub	1266	(CACATTCTCCTGATGATT)₂CACATTCTC=0.5782	delC(TGA)₂TTCACATTCTC=0.4218
1000Genomes_30x	South Asian	Sub	1202	(CACATTCTCCTGATGATT)₂CACATTCTC=0.6464	delC(TGA)₂TTCACATTCTC=0.3536
1000Genomes_30x	East Asian	Sub	1170	(CACATTCTCCTGATGATT)₂CACATTCTC=0.9350	delC(TGA)₂TTCACATTCTC=0.0650
1000Genomes_30x	American	Sub	980	(CACATTCTCCTGATGATT)₂CACATTCTC=0.734	delC(TGA)₂TTCACATTCTC=0.266
1000Genomes	Global	Study-wide	5008	(CACATTCTCCTGATGATT)₂CACATTCTC=0.6727	delC(TGA)₂TTCACATTCTC=0.3273
1000Genomes	African	Sub	1322	(CACATTCTCCTGATGATT)₂CACATTCTC=0.4796	delC(TGA)₂TTCACATTCTC=0.5204
1000Genomes	East Asian	Sub	1008	(CACATTCTCCTGATGATT)₂CACATTCTC=0.9345	delC(TGA)₂TTCACATTCTC=0.0655
1000Genomes	Europe	Sub	1006	(CACATTCTCCTGATGATT)₂CACATTCTC=0.6093	delC(TGA)₂TTCACATTCTC=0.3907
1000Genomes	South Asian	Sub	978	(CACATTCTCCTGATGATT)₂CACATTCTC=0.678	delC(TGA)₂TTCACATTCTC=0.322
1000Genomes	American	Sub	694	(CACATTCTCCTGATGATT)₂CACATTCTC=0.745	delC(TGA)₂TTCACATTCTC=0.255
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(CACATTCTCCTGATGATT)₂CACATTCTC=0.5911	delC(TGA)₂TTCACATTCTC=0.4089
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(CACATTCTCCTGATGATT)₂CACATTCTC=0.6036	delC(TGA)₂TTCACATTCTC=0.3964
Korean Genome Project	KOREAN	Study-wide	1832	(CACATTCTCCTGATGATT)₂CACATTCTC=0.9558	delC(TGA)₂TTCACATTCTC=0.0442
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	(CACATTCTCCTGATGATT)₂CACATTCTC=0.609	delC(TGA)₂TTCACATTCTC=0.391
Northern Sweden	ACPOP	Study-wide	600	(CACATTCTCCTGATGATT)₂CACATTCTC=0.628	delC(TGA)₂TTCACATTCTC=0.372
The Danish reference pan genome	Danish	Study-wide	40	(CACATTCTCCTGATGATT)₂CACATTCTC=0.85	delC(TGA)₂TTCACATTCTC=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 8	NC_000008.11:g.74834870CTGATGATTCACATTCTC[1]
GRCh38.p14 chr 8	NC_000008.11:g.74834870CTGATGATTCACATTCTC[3]
GRCh37.p13 chr 8	NC_000008.10:g.75747105CTGATGATTCACATTCTC[1]
GRCh37.p13 chr 8	NC_000008.10:g.75747105CTGATGATTCACATTCTC[3]

Gene: PI15, peptidase inhibitor 15 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PI15 transcript variant 2	NM_001324403.2:c.274-9093… NM_001324403.2:c.274-9093_274-9076del	N/A	Intron Variant
PI15 transcript variant 1	NM_015886.5:c.274-9093_27… NM_015886.5:c.274-9093_274-9076del	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	(CACATTCTCCTGATGATT)₂CACATTCTC=	delC(TGA)₂TTCACATTCTC	dupC(TGA)₂TTCACATTCTC
GRCh38.p14 chr 8	NC_000008.11:g.74834861_74834905=	NC_000008.11:g.74834870CTGATGATTCACATTCTC[1]	NC_000008.11:g.74834870CTGATGATTCACATTCTC[3]
GRCh37.p13 chr 8	NC_000008.10:g.75747096_75747140=	NC_000008.10:g.75747105CTGATGATTCACATTCTC[1]	NC_000008.10:g.75747105CTGATGATTCACATTCTC[3]
PI15 transcript variant 2	NM_001324403.2:c.274-9120=	NM_001324403.2:c.274-9093_274-9076del	NM_001324403.2:c.274-9120CACATTCTCCTGATGATT[3]
PI15 transcript	NM_015886.3:c.274-9120=	NM_015886.3:c.274-9093_274-9076del	NM_015886.3:c.274-9120CACATTCTCCTGATGATT[3]
PI15 transcript variant 1	NM_015886.5:c.274-9120=	NM_015886.5:c.274-9093_274-9076del	NM_015886.5:c.274-9120CACATTCTCCTGATGATT[3]
PI15 transcript variant X1	XM_005251255.1:c.18+8518=	XM_005251255.1:c.18+8545_18+8562del	XM_005251255.1:c.18+8518CACATTCTCCTGATGATT[3]

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, 14 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss77870175	Dec 06, 2007 (129)
2	HGSV	ss77933049	Dec 06, 2007 (129)
3	HUMANGENOME_JCVI	ss95495981	Feb 06, 2009 (130)
4	HUMANGENOME_JCVI	ss98028389	Feb 05, 2009 (130)
5	1000GENOMES	ss327065124	May 09, 2011 (135)
6	1000GENOMES	ss327128133	May 09, 2011 (135)
7	1000GENOMES	ss327458513	May 09, 2011 (135)
8	1000GENOMES	ss500201874	May 04, 2012 (137)
9	LUNTER	ss551859960	Apr 25, 2013 (138)
10	LUNTER	ss552078470	Apr 25, 2013 (138)
11	LUNTER	ss553346074	Apr 25, 2013 (138)
12	BILGI_BIOE	ss666442116	Apr 25, 2013 (138)
13	EVA-GONL	ss985675238	Aug 21, 2014 (142)
14	1000GENOMES	ss1367980362	Aug 21, 2014 (142)
15	DDI	ss1536590559	Apr 01, 2015 (144)
16	EVA_GENOME_DK	ss1578800736	Apr 01, 2015 (144)
17	EVA_UK10K_ALSPAC	ss1706109078	Apr 01, 2015 (144)
18	EVA_UK10K_TWINSUK	ss1706109243	Apr 01, 2015 (144)
19	HAMMER_LAB	ss1805601589	Sep 08, 2015 (146)
20	JJLAB	ss2030917378	Sep 14, 2016 (149)
21	SWEGEN	ss3003423872	Nov 08, 2017 (151)
22	MCHAISSO	ss3065192644	Nov 08, 2017 (151)
23	MCHAISSO	ss3066209079	Nov 08, 2017 (151)
24	BEROUKHIMLAB	ss3644264404	Oct 12, 2018 (152)
25	URBANLAB	ss3648944848	Oct 12, 2018 (152)
26	EVA_DECODE	ss3722310521	Jul 13, 2019 (153)
27	ACPOP	ss3735792932	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3811340614	Jul 13, 2019 (153)
29	EVA	ss3831236952	Apr 26, 2020 (154)
30	EVA	ss3839127495	Apr 26, 2020 (154)
31	EVA	ss3844587652	Apr 26, 2020 (154)
32	KOGIC	ss3964160916	Apr 26, 2020 (154)
33	GNOMAD	ss4187059377	Apr 26, 2021 (155)
34	GNOMAD	ss4187059379	Apr 26, 2021 (155)
35	TOPMED	ss4791495501	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5189386177	Apr 26, 2021 (155)
37	1000G_HIGH_COVERAGE	ss5277676080	Oct 14, 2022 (156)
38	HUGCELL_USP	ss5474187638	Oct 14, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5568326763	Oct 14, 2022 (156)
40	SANFORD_IMAGENETICS	ss5645686374	Oct 14, 2022 (156)
41	TOMMO_GENOMICS	ss5731648911	Oct 14, 2022 (156)
42	YY_MCH	ss5809837279	Oct 14, 2022 (156)
43	EVA	ss5830740967	Oct 14, 2022 (156)
44	EVA	ss5856432161	Oct 14, 2022 (156)
45	EVA	ss5889579417	Oct 14, 2022 (156)
46	EVA	ss5974908283	Oct 14, 2022 (156)
47	1000Genomes	NC_000008.10 - 75747096	Oct 12, 2018 (152)
48	1000Genomes_30x	NC_000008.11 - 74834861	Oct 14, 2022 (156)
49	The Avon Longitudinal Study of Parents and Children	NC_000008.10 - 75747096	Oct 12, 2018 (152)
50	The Danish reference pan genome	NC_000008.10 - 75747096	Apr 26, 2020 (154)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 300492407 (NC_000008.11:74834860::CACATTCTCCTGATGATT 4/139878) Row 300492409 (NC_000008.11:74834860:CACATTCTCCTGATGATT: 61218/139728)	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 300492407 (NC_000008.11:74834860::CACATTCTCCTGATGATT 4/139878) Row 300492409 (NC_000008.11:74834860:CACATTCTCCTGATGATT: 61218/139728)	-	Apr 26, 2021 (155)
53	Genome of the Netherlands Release 5	NC_000008.10 - 75747096	Apr 26, 2020 (154)
54	Korean Genome Project	NC_000008.11 - 74834861	Apr 26, 2020 (154)
55	Northern Sweden	NC_000008.10 - 75747096	Jul 13, 2019 (153)
56	8.3KJPN	NC_000008.10 - 75747096	Apr 26, 2021 (155)
57	14KJPN	NC_000008.11 - 74834861	Oct 14, 2022 (156)
58	TopMed	NC_000008.11 - 74834861	Apr 26, 2021 (155)
59	UK 10K study - Twins	NC_000008.10 - 75747096	Oct 12, 2018 (152)
60	ALFA	NC_000008.11 - 74834861	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)
rs67423925	Feb 27, 2009 (130)
rs142236288	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss327065124, ss327128133, ss327458513, ss551859960, ss552078470, ss553346074	NC_000008.9:75909650:CACATTCTCCTGA… NC_000008.9:75909650:CACATTCTCCTGATGATT:	NC_000008.11:74834860:CACATTCTCCTG… NC_000008.11:74834860:CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC:CACATTCTCCTGATGATTCACATTCTC	(self)
ss77870175, ss77933049	NC_000008.9:75909677:CTGATGATTCACA… NC_000008.9:75909677:CTGATGATTCACATTCTC:	NC_000008.11:74834860:CACATTCTCCTG… NC_000008.11:74834860:CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC:CACATTCTCCTGATGATTCACATTCTC	(self)
42614344, 23701849, 107704, 10579819, 9077797, 47355484, 23701849, ss500201874, ss666442116, ss985675238, ss1367980362, ss1536590559, ss1578800736, ss1706109078, ss1706109243, ss1805601589, ss2030917378, ss3003423872, ss3644264404, ss3735792932, ss3831236952, ss3839127495, ss5189386177, ss5645686374, ss5830740967, ss5974908283	NC_000008.10:75747095:CACATTCTCCTG… NC_000008.10:75747095:CACATTCTCCTGATGATT:	NC_000008.11:74834860:CACATTCTCCTG… NC_000008.11:74834860:CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC:CACATTCTCCTGATGATTCACATTCTC	(self)
55852698, 20538917, 65486015, 628873061, ss3065192644, ss3066209079, ss3648944848, ss3722310521, ss3811340614, ss3844587652, ss3964160916, ss4187059379, ss4791495501, ss5277676080, ss5474187638, ss5568326763, ss5731648911, ss5809837279, ss5856432161, ss5889579417	NC_000008.11:74834860:CACATTCTCCTG… NC_000008.11:74834860:CACATTCTCCTGATGATT:	NC_000008.11:74834860:CACATTCTCCTG… NC_000008.11:74834860:CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC:CACATTCTCCTGATGATTCACATTCTC	(self)
13499446427	NC_000008.11:74834860:CACATTCTCCTG… NC_000008.11:74834860:CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC:CACATTCTCCTGATGATTCACATTCTC	NC_000008.11:74834860:CACATTCTCCTG… NC_000008.11:74834860:CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC:CACATTCTCCTGATGATTCACATTCTC	(self)
ss98028389	NT_008183.19:27611496:CACATTCTCCTG… NT_008183.19:27611496:CACATTCTCCTGATGATT:	NC_000008.11:74834860:CACATTCTCCTG… NC_000008.11:74834860:CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC:CACATTCTCCTGATGATTCACATTCTC	(self)
ss95495981	NT_008183.19:27611523:CTGATGATTCAC… NT_008183.19:27611523:CTGATGATTCACATTCTC:	NC_000008.11:74834860:CACATTCTCCTG… NC_000008.11:74834860:CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC:CACATTCTCCTGATGATTCACATTCTC	(self)
ss4187059377	NC_000008.11:74834860::CACATTCTCCT… NC_000008.11:74834860::CACATTCTCCTGATGATT	NC_000008.11:74834860:CACATTCTCCTG… NC_000008.11:74834860:CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC:CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC	(self)
13499446427	NC_000008.11:74834860:CACATTCTCCTG… NC_000008.11:74834860:CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC:CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC	NC_000008.11:74834860:CACATTCTCCTG… NC_000008.11:74834860:CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC:CACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTCCTGATGATTCACATTCTC	(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 rs55730814

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

rs55730814