Name: rs200960725
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.

rs200960725

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:139116364-139116375 (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: delAA / delA / dupA / dupAA
Variation Type: Indel Insertion and Deletion
Frequency: dupA=0.00022 (4/18291, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ELF2 : 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	HTRZ	HWEP
Total	Global	18291	AAAAAAAAAAAA=0.99967	AAAAAAAAAA=0.00000, AAAAAAAAAAA=0.00011, AAAAAAAAAAAAA=0.00022, AAAAAAAAAAAAAA=0.00000	0.999562	0.000438	0
European	Sub	14089	AAAAAAAAAAAA=0.99957	AAAAAAAAAA=0.00000, AAAAAAAAAAA=0.00014, AAAAAAAAAAAAA=0.00028, AAAAAAAAAAAAAA=0.00000	0.999431	0.000569	0
African	Sub	2758	AAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000	1.0	0.0	N/A
African Others	Sub	106	AAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	1.0	0.0	N/A
African American	Sub	2652	AAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000	1.0	0.0	N/A
Asian	Sub	102	AAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	1.0	0.0	N/A
East Asian	Sub	80	AAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	1.0	0.0	N/A
Other Asian	Sub	22	AAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	1.0	0.0	N/A
Latin American 1	Sub	144	AAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	1.0	0.0	N/A
Latin American 2	Sub	604	AAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	1.0	0.0	N/A
South Asian	Sub	98	AAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	1.0	0.0	N/A
Other	Sub	496	AAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	1.0	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	18291	(A)₁₂=0.99967	delAA=0.00000, delA=0.00011, dupA=0.00022, dupAA=0.00000
Allele Frequency Aggregator	European	Sub	14089	(A)₁₂=0.99957	delAA=0.00000, delA=0.00014, dupA=0.00028, dupAA=0.00000
Allele Frequency Aggregator	African	Sub	2758	(A)₁₂=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	604	(A)₁₂=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	496	(A)₁₂=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	144	(A)₁₂=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Asian	Sub	102	(A)₁₂=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	South Asian	Sub	98	(A)₁₂=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00

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 4	NC_000004.12:g.139116374_139116375del
GRCh38.p14 chr 4	NC_000004.12:g.139116375del
GRCh38.p14 chr 4	NC_000004.12:g.139116375dup
GRCh38.p14 chr 4	NC_000004.12:g.139116374_139116375dup
GRCh37.p13 chr 4	NC_000004.11:g.140037528_140037529del
GRCh37.p13 chr 4	NC_000004.11:g.140037529del
GRCh37.p13 chr 4	NC_000004.11:g.140037529dup
GRCh37.p13 chr 4	NC_000004.11:g.140037528_140037529dup

Gene: ELF2, E74 like ETS transcription factor 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ELF2 transcript variant 6	NM_001331036.3:c.238+8799… NM_001331036.3:c.238+8799_238+8800del	N/A	Intron Variant
ELF2 transcript variant 7	NM_001371324.1:c.238+8799… NM_001371324.1:c.238+8799_238+8800del	N/A	Intron Variant
ELF2 transcript variant 8	NM_001371336.1:c.238+8799… NM_001371336.1:c.238+8799_238+8800del	N/A	Intron Variant
ELF2 transcript variant 9	NM_001371337.1:c.-75+284_… NM_001371337.1:c.-75+284_-75+285del	N/A	Intron Variant
ELF2 transcript variant 10	NM_001371338.1:c.-75+284_… NM_001371338.1:c.-75+284_-75+285del	N/A	Intron Variant
ELF2 transcript variant 11	NM_001371339.1:c.-75+284_… NM_001371339.1:c.-75+284_-75+285del	N/A	Intron Variant
ELF2 transcript variant 1	NM_201999.3:c.238+8799_23… NM_201999.3:c.238+8799_238+8800del	N/A	Intron Variant
ELF2 transcript variant 3	NM_001276457.2:c.	N/A	Genic Upstream Transcript Variant
ELF2 transcript variant 4	NM_001276458.3:c.	N/A	Genic Upstream Transcript Variant
ELF2 transcript variant 5	NM_001276459.3:c.	N/A	Genic Upstream Transcript Variant
ELF2 transcript variant 2	NM_006874.5:c.	N/A	Genic Upstream Transcript Variant
ELF2 transcript variant X10	XM_005262805.3:c.238+8799… XM_005262805.3:c.238+8799_238+8800del	N/A	Intron Variant
ELF2 transcript variant X11	XM_011531711.3:c.-75+284_… XM_011531711.3:c.-75+284_-75+285del	N/A	Intron Variant
ELF2 transcript variant X1	XM_047449732.1:c.238+8799… XM_047449732.1:c.238+8799_238+8800del	N/A	Intron Variant
ELF2 transcript variant X2	XM_047449733.1:c.238+8799… XM_047449733.1:c.238+8799_238+8800del	N/A	Intron Variant
ELF2 transcript variant X3	XM_047449734.1:c.238+8799… XM_047449734.1:c.238+8799_238+8800del	N/A	Intron Variant
ELF2 transcript variant X4	XM_047449736.1:c.238+8799… XM_047449736.1:c.238+8799_238+8800del	N/A	Intron Variant
ELF2 transcript variant X5	XM_047449737.1:c.238+8799… XM_047449737.1:c.238+8799_238+8800del	N/A	Intron Variant
ELF2 transcript variant X6	XM_047449738.1:c.238+8799… XM_047449738.1:c.238+8799_238+8800del	N/A	Intron Variant
ELF2 transcript variant X7	XM_047449739.1:c.238+8799… XM_047449739.1:c.238+8799_238+8800del	N/A	Intron Variant
ELF2 transcript variant X8	XM_047449740.1:c.238+8799… XM_047449740.1:c.238+8799_238+8800del	N/A	Intron Variant
ELF2 transcript variant X9	XM_047449741.1:c.238+8799… XM_047449741.1:c.238+8799_238+8800del	N/A	Intron Variant
ELF2 transcript variant X13	XM_011531714.3:c.	N/A	Genic Upstream Transcript Variant
ELF2 transcript variant X12	XM_047449742.1:c.	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	(A)₁₂=	delAA	delA	dupA	dupAA
GRCh38.p14 chr 4	NC_000004.12:g.139116364_139116375=	NC_000004.12:g.139116374_139116375del	NC_000004.12:g.139116375del	NC_000004.12:g.139116375dup	NC_000004.12:g.139116374_139116375dup
GRCh37.p13 chr 4	NC_000004.11:g.140037518_140037529=	NC_000004.11:g.140037528_140037529del	NC_000004.11:g.140037529del	NC_000004.11:g.140037529dup	NC_000004.11:g.140037528_140037529dup
ELF2 transcript variant 6	NM_001331036.3:c.238+8800=	NM_001331036.3:c.238+8799_238+8800del	NM_001331036.3:c.238+8800del	NM_001331036.3:c.238+8800dup	NM_001331036.3:c.238+8799_238+8800dup
ELF2 transcript variant 7	NM_001371324.1:c.238+8800=	NM_001371324.1:c.238+8799_238+8800del	NM_001371324.1:c.238+8800del	NM_001371324.1:c.238+8800dup	NM_001371324.1:c.238+8799_238+8800dup
ELF2 transcript variant 8	NM_001371336.1:c.238+8800=	NM_001371336.1:c.238+8799_238+8800del	NM_001371336.1:c.238+8800del	NM_001371336.1:c.238+8800dup	NM_001371336.1:c.238+8799_238+8800dup
ELF2 transcript variant 9	NM_001371337.1:c.-75+285=	NM_001371337.1:c.-75+284_-75+285del	NM_001371337.1:c.-75+285del	NM_001371337.1:c.-75+285dup	NM_001371337.1:c.-75+284_-75+285dup
ELF2 transcript variant 10	NM_001371338.1:c.-75+285=	NM_001371338.1:c.-75+284_-75+285del	NM_001371338.1:c.-75+285del	NM_001371338.1:c.-75+285dup	NM_001371338.1:c.-75+284_-75+285dup
ELF2 transcript variant 11	NM_001371339.1:c.-75+285=	NM_001371339.1:c.-75+284_-75+285del	NM_001371339.1:c.-75+285del	NM_001371339.1:c.-75+285dup	NM_001371339.1:c.-75+284_-75+285dup
ELF2 transcript variant 1	NM_201999.2:c.238+8800=	NM_201999.2:c.238+8799_238+8800del	NM_201999.2:c.238+8800del	NM_201999.2:c.238+8800dup	NM_201999.2:c.238+8799_238+8800dup
ELF2 transcript variant 1	NM_201999.3:c.238+8800=	NM_201999.3:c.238+8799_238+8800del	NM_201999.3:c.238+8800del	NM_201999.3:c.238+8800dup	NM_201999.3:c.238+8799_238+8800dup
ELF2 transcript variant X1	XM_005262803.1:c.238+8800=	XM_005262803.1:c.238+8799_238+8800del	XM_005262803.1:c.238+8800del	XM_005262803.1:c.238+8800dup	XM_005262803.1:c.238+8799_238+8800dup
ELF2 transcript variant X2	XM_005262804.1:c.238+8800=	XM_005262804.1:c.238+8799_238+8800del	XM_005262804.1:c.238+8800del	XM_005262804.1:c.238+8800dup	XM_005262804.1:c.238+8799_238+8800dup
ELF2 transcript variant X4	XM_005262805.1:c.238+8800=	XM_005262805.1:c.238+8799_238+8800del	XM_005262805.1:c.238+8800del	XM_005262805.1:c.238+8800dup	XM_005262805.1:c.238+8799_238+8800dup
ELF2 transcript variant X10	XM_005262805.3:c.238+8800=	XM_005262805.3:c.238+8799_238+8800del	XM_005262805.3:c.238+8800del	XM_005262805.3:c.238+8800dup	XM_005262805.3:c.238+8799_238+8800dup
ELF2 transcript variant X4	XM_005262806.1:c.-75+285=	XM_005262806.1:c.-75+284_-75+285del	XM_005262806.1:c.-75+285del	XM_005262806.1:c.-75+285dup	XM_005262806.1:c.-75+284_-75+285dup
ELF2 transcript variant X11	XM_011531711.3:c.-75+285=	XM_011531711.3:c.-75+284_-75+285del	XM_011531711.3:c.-75+285del	XM_011531711.3:c.-75+285dup	XM_011531711.3:c.-75+284_-75+285dup
ELF2 transcript variant X1	XM_047449732.1:c.238+8800=	XM_047449732.1:c.238+8799_238+8800del	XM_047449732.1:c.238+8800del	XM_047449732.1:c.238+8800dup	XM_047449732.1:c.238+8799_238+8800dup
ELF2 transcript variant X2	XM_047449733.1:c.238+8800=	XM_047449733.1:c.238+8799_238+8800del	XM_047449733.1:c.238+8800del	XM_047449733.1:c.238+8800dup	XM_047449733.1:c.238+8799_238+8800dup
ELF2 transcript variant X3	XM_047449734.1:c.238+8800=	XM_047449734.1:c.238+8799_238+8800del	XM_047449734.1:c.238+8800del	XM_047449734.1:c.238+8800dup	XM_047449734.1:c.238+8799_238+8800dup
ELF2 transcript variant X4	XM_047449736.1:c.238+8800=	XM_047449736.1:c.238+8799_238+8800del	XM_047449736.1:c.238+8800del	XM_047449736.1:c.238+8800dup	XM_047449736.1:c.238+8799_238+8800dup
ELF2 transcript variant X5	XM_047449737.1:c.238+8800=	XM_047449737.1:c.238+8799_238+8800del	XM_047449737.1:c.238+8800del	XM_047449737.1:c.238+8800dup	XM_047449737.1:c.238+8799_238+8800dup
ELF2 transcript variant X6	XM_047449738.1:c.238+8800=	XM_047449738.1:c.238+8799_238+8800del	XM_047449738.1:c.238+8800del	XM_047449738.1:c.238+8800dup	XM_047449738.1:c.238+8799_238+8800dup
ELF2 transcript variant X7	XM_047449739.1:c.238+8800=	XM_047449739.1:c.238+8799_238+8800del	XM_047449739.1:c.238+8800del	XM_047449739.1:c.238+8800dup	XM_047449739.1:c.238+8799_238+8800dup
ELF2 transcript variant X8	XM_047449740.1:c.238+8800=	XM_047449740.1:c.238+8799_238+8800del	XM_047449740.1:c.238+8800del	XM_047449740.1:c.238+8800dup	XM_047449740.1:c.238+8799_238+8800dup
ELF2 transcript variant X9	XM_047449741.1:c.238+8800=	XM_047449741.1:c.238+8799_238+8800del	XM_047449741.1:c.238+8800del	XM_047449741.1:c.238+8800dup	XM_047449741.1:c.238+8799_238+8800dup

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#.

19 SubSNP, 8 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GMI	ss288583469	May 04, 2012 (137)
2	GMI	ss288583470	May 04, 2012 (137)
3	SSMP	ss663463094	Apr 01, 2015 (144)
4	JJLAB	ss2030635368	Sep 14, 2016 (149)
5	SWEGEN	ss2995665316	Nov 08, 2017 (151)
6	BIOINF_KMB_FNS_UNIBA	ss3645830732	Oct 12, 2018 (152)
7	GNOMAD	ss4121578866	Apr 26, 2021 (155)
8	GNOMAD	ss4121578867	Apr 26, 2021 (155)
9	GNOMAD	ss4121578868	Apr 26, 2021 (155)
10	TOMMO_GENOMICS	ss5168305629	Apr 26, 2021 (155)
11	TOMMO_GENOMICS	ss5168305630	Apr 26, 2021 (155)
12	1000G_HIGH_COVERAGE	ss5261254767	Oct 17, 2022 (156)
13	1000G_HIGH_COVERAGE	ss5261254768	Oct 17, 2022 (156)
14	HUGCELL_USP	ss5459788745	Oct 17, 2022 (156)
15	HUGCELL_USP	ss5459788746	Oct 17, 2022 (156)
16	TOMMO_GENOMICS	ss5703379114	Oct 17, 2022 (156)
17	TOMMO_GENOMICS	ss5703379115	Oct 17, 2022 (156)
18	YY_MCH	ss5805597387	Oct 17, 2022 (156)
19	EVA	ss5854475263	Oct 17, 2022 (156)
20	gnomAD - Genomes Submission ignored due to conflicting rows: Row 166920317 (NC_000004.12:139116363::A 692/119412) Row 166920318 (NC_000004.12:139116363:A: 803/119020) Row 166920319 (NC_000004.12:139116363:AA: 5/119440)	-	Apr 26, 2021 (155)
21	gnomAD - Genomes Submission ignored due to conflicting rows: Row 166920317 (NC_000004.12:139116363::A 692/119412) Row 166920318 (NC_000004.12:139116363:A: 803/119020) Row 166920319 (NC_000004.12:139116363:AA: 5/119440)	-	Apr 26, 2021 (155)
22	gnomAD - Genomes Submission ignored due to conflicting rows: Row 166920317 (NC_000004.12:139116363::A 692/119412) Row 166920318 (NC_000004.12:139116363:A: 803/119020) Row 166920319 (NC_000004.12:139116363:AA: 5/119440)	-	Apr 26, 2021 (155)
23	8.3KJPN Submission ignored due to conflicting rows: Row 26274936 (NC_000004.11:140037517::A 191/16760) Row 26274937 (NC_000004.11:140037517:A: 11/16760)	-	Apr 26, 2021 (155)
24	8.3KJPN Submission ignored due to conflicting rows: Row 26274936 (NC_000004.11:140037517::A 191/16760) Row 26274937 (NC_000004.11:140037517:A: 11/16760)	-	Apr 26, 2021 (155)
25	14KJPN Submission ignored due to conflicting rows: Row 37216218 (NC_000004.12:139116363:A: 8/28258) Row 37216219 (NC_000004.12:139116363::A 296/28258)	-	Oct 17, 2022 (156)
26	14KJPN Submission ignored due to conflicting rows: Row 37216218 (NC_000004.12:139116363:A: 8/28258) Row 37216219 (NC_000004.12:139116363::A 296/28258)	-	Oct 17, 2022 (156)
27	ALFA	NC_000004.12 - 139116364	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)
rs368957270	May 15, 2013 (138)
rs1049228779	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4121578868	NC_000004.12:139116363:AA:	NC_000004.12:139116363:AAAAAAAAAAA… NC_000004.12:139116363:AAAAAAAAAAAA:AAAAAAAAAA	(self)
7101351558	NC_000004.12:139116363:AAAAAAAAAAA… NC_000004.12:139116363:AAAAAAAAAAAA:AAAAAAAAAA	NC_000004.12:139116363:AAAAAAAAAAA… NC_000004.12:139116363:AAAAAAAAAAAA:AAAAAAAAAA	(self)
ss288583469	NC_000004.10:140256978:A:	NC_000004.12:139116363:AAAAAAAAAAA… NC_000004.12:139116363:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss2030635368, ss5168305630	NC_000004.11:140037517:A:	NC_000004.12:139116363:AAAAAAAAAAA… NC_000004.12:139116363:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3645830732, ss4121578867, ss5261254767, ss5459788745, ss5703379114	NC_000004.12:139116363:A:	NC_000004.12:139116363:AAAAAAAAAAA… NC_000004.12:139116363:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
7101351558	NC_000004.12:139116363:AAAAAAAAAAA… NC_000004.12:139116363:AAAAAAAAAAAA:AAAAAAAAAAA	NC_000004.12:139116363:AAAAAAAAAAA… NC_000004.12:139116363:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss288583470	NC_000004.10:140256979::A	NC_000004.12:139116363:AAAAAAAAAAA… NC_000004.12:139116363:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss663463094, ss2995665316, ss5168305629	NC_000004.11:140037517::A	NC_000004.12:139116363:AAAAAAAAAAA… NC_000004.12:139116363:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4121578866, ss5261254768, ss5459788746, ss5703379115, ss5805597387, ss5854475263	NC_000004.12:139116363::A	NC_000004.12:139116363:AAAAAAAAAAA… NC_000004.12:139116363:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
7101351558	NC_000004.12:139116363:AAAAAAAAAAA… NC_000004.12:139116363:AAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000004.12:139116363:AAAAAAAAAAA… NC_000004.12:139116363:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
7101351558	NC_000004.12:139116363:AAAAAAAAAAA… NC_000004.12:139116363:AAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000004.12:139116363:AAAAAAAAAAA… NC_000004.12:139116363:AAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2435590544	NC_000004.11:140037517:AA:	NC_000004.12:139116363:AAAAAAAAAAA… NC_000004.12:139116363:AAAAAAAAAAAA:AAAAAAAAAA
ss3444509748	NC_000004.12:139116363::AA	NC_000004.12:139116363:AAAAAAAAAAA… NC_000004.12:139116363:AAAAAAAAAAAA:AAAAAAAAAAAAAA

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

No publications for rs200960725

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

rs200960725