Name: rs57133101
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.

rs57133101

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:117406755-117406766 (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: delAAA / delAA / delA / dupA / dup…
delAAA / delAA / delA / dupA / dupAA
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.11565 (1203/10402, ALFA)
delA=0.1788 (689/3854, ALSPAC)
delA=0.1872 (714/3814, 1000G) (+ 1 more)
delA=0.1944 (721/3708, TWINSUK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ASZ1 : 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	10402	AAAAAAAAAAAA=0.84022	AAAAAAAAAA=0.00000, AAAAAAAAAAA=0.11565, AAAAAAAAAAAAA=0.04413, AAAAAAAAAAAAAA=0.00000	0.810142	0.036253	0.153604	32
European	Sub	8534	AAAAAAAAAAAA=0.8054	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.1408, AAAAAAAAAAAAA=0.0538, AAAAAAAAAAAAAA=0.0000	0.7642	0.045076	0.190724	32
African	Sub	1382	AAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	40	AAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1342	AAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	20	AAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	14	AAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	6	AAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	72	AAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	170	AAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	32	AAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	192	AAAAAAAAAAAA=0.995	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.005, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	0.989583	0.0	0.010417	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	10402	(A)₁₂=0.84022	delAA=0.00000, delA=0.11565, dupA=0.04413, dupAA=0.00000
Allele Frequency Aggregator	European	Sub	8534	(A)₁₂=0.8054	delAA=0.0000, delA=0.1408, dupA=0.0538, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	1382	(A)₁₂=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Other	Sub	192	(A)₁₂=0.995	delAA=0.000, delA=0.005, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	170	(A)₁₂=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	72	(A)₁₂=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	32	(A)₁₂=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	20	(A)₁₂=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₁₂=0.8212	delA=0.1788
1000Genomes	Global	Study-wide	3814	(A)₁₂=0.8128	delA=0.1872
1000Genomes	African	Sub	1166	(A)₁₂=0.7479	delA=0.2521
1000Genomes	Europe	Sub	920	(A)₁₂=0.765	delA=0.235
1000Genomes	South Asian	Sub	615	(A)₁₂=0.878	delA=0.122
1000Genomes	East Asian	Sub	604	(A)₁₂=0.952	delA=0.048
1000Genomes	American	Sub	509	(A)₁₂=0.804	delA=0.196
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(A)₁₂=0.8056	delA=0.1944

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 7	NC_000007.14:g.117406764_117406766del
GRCh38.p14 chr 7	NC_000007.14:g.117406765_117406766del
GRCh38.p14 chr 7	NC_000007.14:g.117406766del
GRCh38.p14 chr 7	NC_000007.14:g.117406766dup
GRCh38.p14 chr 7	NC_000007.14:g.117406765_117406766dup
GRCh37.p13 chr 7	NC_000007.13:g.117046818_117046820del
GRCh37.p13 chr 7	NC_000007.13:g.117046819_117046820del
GRCh37.p13 chr 7	NC_000007.13:g.117046820del
GRCh37.p13 chr 7	NC_000007.13:g.117046820dup
GRCh37.p13 chr 7	NC_000007.13:g.117046819_117046820dup

Gene: ASZ1, ankyrin repeat, SAM and basic leucine zipper domain containing 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ASZ1 transcript variant 3	NM_001301821.2:c.440+1340… NM_001301821.2:c.440+13406_440+13408del	N/A	Intron Variant
ASZ1 transcript variant 4	NM_001301822.2:c.-73+1340… NM_001301822.2:c.-73+13406_-73+13408del	N/A	Intron Variant
ASZ1 transcript variant 1	NM_130768.3:c.440+13406_4… NM_130768.3:c.440+13406_440+13408del	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)₁₂=	delAAA	delAA	delA	dupA	dupAA
GRCh38.p14 chr 7	NC_000007.14:g.117406755_117406766=	NC_000007.14:g.117406764_117406766del	NC_000007.14:g.117406765_117406766del	NC_000007.14:g.117406766del	NC_000007.14:g.117406766dup	NC_000007.14:g.117406765_117406766dup
GRCh37.p13 chr 7	NC_000007.13:g.117046809_117046820=	NC_000007.13:g.117046818_117046820del	NC_000007.13:g.117046819_117046820del	NC_000007.13:g.117046820del	NC_000007.13:g.117046820dup	NC_000007.13:g.117046819_117046820dup
ASZ1 transcript variant 3	NM_001301821.2:c.440+13408=	NM_001301821.2:c.440+13406_440+13408del	NM_001301821.2:c.440+13407_440+13408del	NM_001301821.2:c.440+13408del	NM_001301821.2:c.440+13408dup	NM_001301821.2:c.440+13407_440+13408dup
ASZ1 transcript variant 4	NM_001301822.2:c.-73+13408=	NM_001301822.2:c.-73+13406_-73+13408del	NM_001301822.2:c.-73+13407_-73+13408del	NM_001301822.2:c.-73+13408del	NM_001301822.2:c.-73+13408dup	NM_001301822.2:c.-73+13407_-73+13408dup
ASZ1 transcript variant 1	NM_130768.2:c.440+13408=	NM_130768.2:c.440+13406_440+13408del	NM_130768.2:c.440+13407_440+13408del	NM_130768.2:c.440+13408del	NM_130768.2:c.440+13408dup	NM_130768.2:c.440+13407_440+13408dup
ASZ1 transcript variant 1	NM_130768.3:c.440+13408=	NM_130768.3:c.440+13406_440+13408del	NM_130768.3:c.440+13407_440+13408del	NM_130768.3:c.440+13408del	NM_130768.3:c.440+13408dup	NM_130768.3:c.440+13407_440+13408dup

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#.

53 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42925779	Dec 03, 2013 (138)
2	HGSV	ss82742836	Dec 14, 2007 (129)
3	GMI	ss287819279	Dec 06, 2013 (142)
4	GMI	ss288867328	Oct 12, 2018 (152)
5	SSMP	ss663738089	Apr 01, 2015 (144)
6	BILGI_BIOE	ss666413703	Apr 25, 2013 (138)
7	1000GENOMES	ss1377594718	Aug 21, 2014 (142)
8	1000GENOMES	ss1377594721	Oct 12, 2018 (152)
9	EVA_UK10K_ALSPAC	ss1705796439	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1705796507	Apr 01, 2015 (144)
11	HAMMER_LAB	ss1805184934	Sep 08, 2015 (146)
12	SYSTEMSBIOZJU	ss2626824962	Nov 08, 2017 (151)
13	SWEGEN	ss3001908310	Nov 08, 2017 (151)
14	MCHAISSO	ss3066165966	Nov 08, 2017 (151)
15	BIOINF_KMB_FNS_UNIBA	ss3646053235	Oct 12, 2018 (152)
16	EVA_DECODE	ss3720539138	Jul 13, 2019 (153)
17	EVA_DECODE	ss3720539139	Jul 13, 2019 (153)
18	EVA_DECODE	ss3720539140	Jul 13, 2019 (153)
19	ACPOP	ss3735003281	Jul 13, 2019 (153)
20	ACPOP	ss3735003282	Jul 13, 2019 (153)
21	PACBIO	ss3785937283	Jul 13, 2019 (153)
22	PACBIO	ss3785937284	Jul 13, 2019 (153)
23	PACBIO	ss3791219445	Jul 13, 2019 (153)
24	PACBIO	ss3791219446	Jul 13, 2019 (153)
25	PACBIO	ss3796099565	Jul 13, 2019 (153)
26	PACBIO	ss3796099566	Jul 13, 2019 (153)
27	KHV_HUMAN_GENOMES	ss3810237717	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3810237718	Jul 13, 2019 (153)
29	EVA	ss3830780452	Apr 26, 2020 (154)
30	KOGIC	ss3962432537	Apr 26, 2020 (154)
31	KOGIC	ss3962432538	Apr 26, 2020 (154)
32	KOGIC	ss3962432539	Apr 26, 2020 (154)
33	GNOMAD	ss4171630396	Apr 26, 2021 (155)
34	GNOMAD	ss4171630397	Apr 26, 2021 (155)
35	GNOMAD	ss4171630398	Apr 26, 2021 (155)
36	GNOMAD	ss4171630399	Apr 26, 2021 (155)
37	GNOMAD	ss4171630400	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5185230696	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5185230697	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5185230698	Apr 26, 2021 (155)
41	1000G_HIGH_COVERAGE	ss5274464051	Oct 13, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5274464052	Oct 13, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5274464053	Oct 13, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5274464054	Oct 13, 2022 (156)
45	HUGCELL_USP	ss5471378399	Oct 13, 2022 (156)
46	HUGCELL_USP	ss5471378400	Oct 13, 2022 (156)
47	HUGCELL_USP	ss5471378401	Oct 13, 2022 (156)
48	TOMMO_GENOMICS	ss5726120915	Oct 13, 2022 (156)
49	TOMMO_GENOMICS	ss5726120916	Oct 13, 2022 (156)
50	TOMMO_GENOMICS	ss5726120917	Oct 13, 2022 (156)
51	EVA	ss5823420199	Oct 13, 2022 (156)
52	EVA	ss5856065149	Oct 13, 2022 (156)
53	EVA	ss5973020124	Oct 13, 2022 (156)
54	1000Genomes	NC_000007.13 - 117046809	Oct 12, 2018 (152)
55	The Avon Longitudinal Study of Parents and Children	NC_000007.13 - 117046809	Oct 12, 2018 (152)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 274308726 (NC_000007.14:117406754::A 15462/128842) Row 274308727 (NC_000007.14:117406754::AA 21/128982) Row 274308728 (NC_000007.14:117406754:A: 26683/128776)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 274308726 (NC_000007.14:117406754::A 15462/128842) Row 274308727 (NC_000007.14:117406754::AA 21/128982) Row 274308728 (NC_000007.14:117406754:A: 26683/128776)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 274308726 (NC_000007.14:117406754::A 15462/128842) Row 274308727 (NC_000007.14:117406754::AA 21/128982) Row 274308728 (NC_000007.14:117406754:A: 26683/128776)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 274308726 (NC_000007.14:117406754::A 15462/128842) Row 274308727 (NC_000007.14:117406754::AA 21/128982) Row 274308728 (NC_000007.14:117406754:A: 26683/128776)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 274308726 (NC_000007.14:117406754::A 15462/128842) Row 274308727 (NC_000007.14:117406754::AA 21/128982) Row 274308728 (NC_000007.14:117406754:A: 26683/128776)...	-	Apr 26, 2021 (155)
61	Korean Genome Project Submission ignored due to conflicting rows: Row 18810538 (NC_000007.14:117406755::A 923/1832) Row 18810539 (NC_000007.14:117406755::AA 16/1832) Row 18810540 (NC_000007.14:117406754:A: 43/1832)	-	Apr 26, 2020 (154)
62	Korean Genome Project Submission ignored due to conflicting rows: Row 18810538 (NC_000007.14:117406755::A 923/1832) Row 18810539 (NC_000007.14:117406755::AA 16/1832) Row 18810540 (NC_000007.14:117406754:A: 43/1832)	-	Apr 26, 2020 (154)
63	Korean Genome Project Submission ignored due to conflicting rows: Row 18810538 (NC_000007.14:117406755::A 923/1832) Row 18810539 (NC_000007.14:117406755::AA 16/1832) Row 18810540 (NC_000007.14:117406754:A: 43/1832)	-	Apr 26, 2020 (154)
64	Northern Sweden Submission ignored due to conflicting rows: Row 8288146 (NC_000007.13:117046808:A: 152/600) Row 8288147 (NC_000007.13:117046808::A 45/600)	-	Jul 13, 2019 (153)
65	Northern Sweden Submission ignored due to conflicting rows: Row 8288146 (NC_000007.13:117046808:A: 152/600) Row 8288147 (NC_000007.13:117046808::A 45/600)	-	Jul 13, 2019 (153)
66	8.3KJPN Submission ignored due to conflicting rows: Row 43200003 (NC_000007.13:117046808::A 7449/16758) Row 43200004 (NC_000007.13:117046808:A: 294/16758) Row 43200005 (NC_000007.13:117046808::AA 14/16758)	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 43200003 (NC_000007.13:117046808::A 7449/16758) Row 43200004 (NC_000007.13:117046808:A: 294/16758) Row 43200005 (NC_000007.13:117046808::AA 14/16758)	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 43200003 (NC_000007.13:117046808::A 7449/16758) Row 43200004 (NC_000007.13:117046808:A: 294/16758) Row 43200005 (NC_000007.13:117046808::AA 14/16758)	-	Apr 26, 2021 (155)
69	14KJPN Submission ignored due to conflicting rows: Row 59958019 (NC_000007.14:117406754::A 12363/28258) Row 59958020 (NC_000007.14:117406754:A: 509/28258) Row 59958021 (NC_000007.14:117406754::AA 13/28258)	-	Oct 13, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 59958019 (NC_000007.14:117406754::A 12363/28258) Row 59958020 (NC_000007.14:117406754:A: 509/28258) Row 59958021 (NC_000007.14:117406754::AA 13/28258)	-	Oct 13, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 59958019 (NC_000007.14:117406754::A 12363/28258) Row 59958020 (NC_000007.14:117406754:A: 509/28258) Row 59958021 (NC_000007.14:117406754::AA 13/28258)	-	Oct 13, 2022 (156)
72	UK 10K study - Twins	NC_000007.13 - 117046809	Oct 12, 2018 (152)
73	ALFA	NC_000007.14 - 117406755	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)
rs138657039	May 11, 2012 (137)
rs398111763	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4171630400	NC_000007.14:117406754:AAA:	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAA	(self)
ss3720539140, ss4171630399, ss5274464053	NC_000007.14:117406754:AA:	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAA	(self)
854800334	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAA	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAA	(self)
ss82742836	NC_000007.11:116640770:A:	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
38853894, 21616184, 21616184, ss666413703, ss1377594718, ss1705796439, ss1705796507, ss3001908310, ss3735003281, ss3785937283, ss3791219445, ss3796099565, ss3830780452, ss5185230697, ss5823420199, ss5973020124	NC_000007.13:117046808:A:	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3066165966, ss3646053235, ss3810237717, ss3962432539, ss4171630398, ss5274464052, ss5471378399, ss5726120916	NC_000007.14:117406754:A:	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
854800334	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAA	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3720539139	NC_000007.14:117406755:A:	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss287819279	NT_007933.15:55079651:A:	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss288867328	NC_000007.12:116834056::A	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss663738089, ss1805184934, ss2626824962, ss3735003282, ss3785937284, ss3791219446, ss3796099566, ss5185230696	NC_000007.13:117046808::A	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss1377594721	NC_000007.13:117046809::A	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4171630396, ss5274464051, ss5471378400, ss5726120915, ss5856065149	NC_000007.14:117406754::A	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
854800334	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3810237718, ss3962432537	NC_000007.14:117406755::A	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3720539138	NC_000007.14:117406756::A	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss42925779	NT_007933.15:55079663::A	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5185230698	NC_000007.13:117046808::AA	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4171630397, ss5274464054, ss5471378401, ss5726120917	NC_000007.14:117406754::AA	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
854800334	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3962432538	NC_000007.14:117406755::AA	NC_000007.14:117406754:AAAAAAAAAAA… NC_000007.14:117406754:AAAAAAAAAAAA:AAAAAAAAAAAAAA	(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 rs57133101

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

rs57133101