Name: rs35043860
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.

rs35043860

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:97717623-97717634 (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: delCCC / delCC / delC / dupC / dup…
delCCC / delCC / delC / dupC / dupCC
Variation Type: Indel Insertion and Deletion
Frequency: delC=0.1369 (1212/8854, ALFA)
delC=0.45 (18/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MTDH : 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	8854	CCCCCCCCCCCC=0.8426	CCCCCCCCC=0.0000, CCCCCCCCCC=0.0000, CCCCCCCCCCC=0.1369, CCCCCCCCCCCCC=0.0203, CCCCCCCCCCCCCC=0.0002	0.771872	0.047272	0.180856	32
European	Sub	7644	CCCCCCCCCCCC=0.8178	CCCCCCCCC=0.0000, CCCCCCCCCC=0.0000, CCCCCCCCCCC=0.1584, CCCCCCCCCCCCC=0.0235, CCCCCCCCCCCCCC=0.0003	0.734302	0.055114	0.210584	32
African	Sub	812	CCCCCCCCCCCC=1.000	CCCCCCCCC=0.000, CCCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000	1.0	0.0	0.0	N/A
African Others	Sub	18	CCCCCCCCCCCC=1.00	CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
African American	Sub	794	CCCCCCCCCCCC=1.000	CCCCCCCCC=0.000, CCCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000	1.0	0.0	0.0	N/A
Asian	Sub	10	CCCCCCCCCCCC=1.0	CCCCCCCCC=0.0, CCCCCCCCCC=0.0, CCCCCCCCCCC=0.0, CCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCC=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	10	CCCCCCCCCCCC=1.0	CCCCCCCCC=0.0, CCCCCCCCCC=0.0, CCCCCCCCCCC=0.0, CCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCC=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	CCCCCCCCCCCC=0	CCCCCCCCC=0, CCCCCCCCCC=0, CCCCCCCCCCC=0, CCCCCCCCCCCCC=0, CCCCCCCCCCCCCC=0	0	0	0	N/A
Latin American 1	Sub	50	CCCCCCCCCCCC=1.00	CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	164	CCCCCCCCCCCC=1.000	CCCCCCCCC=0.000, CCCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	22	CCCCCCCCCCCC=1.00	CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Other	Sub	152	CCCCCCCCCCCC=0.993	CCCCCCCCC=0.000, CCCCCCCCCC=0.000, CCCCCCCCCCC=0.007, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000	0.986842	0.0	0.013158	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	8854	(C)₁₂=0.8426	delCCC=0.0000, delCC=0.0000, delC=0.1369, dupC=0.0203, dupCC=0.0002
Allele Frequency Aggregator	European	Sub	7644	(C)₁₂=0.8178	delCCC=0.0000, delCC=0.0000, delC=0.1584, dupC=0.0235, dupCC=0.0003
Allele Frequency Aggregator	African	Sub	812	(C)₁₂=1.000	delCCC=0.000, delCC=0.000, delC=0.000, dupC=0.000, dupCC=0.000
Allele Frequency Aggregator	Latin American 2	Sub	164	(C)₁₂=1.000	delCCC=0.000, delCC=0.000, delC=0.000, dupC=0.000, dupCC=0.000
Allele Frequency Aggregator	Other	Sub	152	(C)₁₂=0.993	delCCC=0.000, delCC=0.000, delC=0.007, dupC=0.000, dupCC=0.000
Allele Frequency Aggregator	Latin American 1	Sub	50	(C)₁₂=1.00	delCCC=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00
Allele Frequency Aggregator	South Asian	Sub	22	(C)₁₂=1.00	delCCC=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00
Allele Frequency Aggregator	Asian	Sub	10	(C)₁₂=1.0	delCCC=0.0, delCC=0.0, delC=0.0, dupC=0.0, dupCC=0.0
The Danish reference pan genome	Danish	Study-wide	40	(C)₁₂=0.55	delC=0.45

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.97717632_97717634del
GRCh38.p14 chr 8	NC_000008.11:g.97717633_97717634del
GRCh38.p14 chr 8	NC_000008.11:g.97717634del
GRCh38.p14 chr 8	NC_000008.11:g.97717634dup
GRCh38.p14 chr 8	NC_000008.11:g.97717633_97717634dup
GRCh37.p13 chr 8	NC_000008.10:g.98729860_98729862del
GRCh37.p13 chr 8	NC_000008.10:g.98729861_98729862del
GRCh37.p13 chr 8	NC_000008.10:g.98729862del
GRCh37.p13 chr 8	NC_000008.10:g.98729862dup
GRCh37.p13 chr 8	NC_000008.10:g.98729861_98729862dup

Gene: MTDH, metadherin (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MTDH transcript variant 2	NM_001363136.1:c.1315-141… NM_001363136.1:c.1315-1417_1315-1415del	N/A	Intron Variant
MTDH transcript variant 3	NM_001363137.1:c.1471-141… NM_001363137.1:c.1471-1417_1471-1415del	N/A	Intron Variant
MTDH transcript variant 4	NM_001363138.1:c.1282-141… NM_001363138.1:c.1282-1417_1282-1415del	N/A	Intron Variant
MTDH transcript variant 5	NM_001363139.1:c.1216-141… NM_001363139.1:c.1216-1417_1216-1415del	N/A	Intron Variant
MTDH transcript variant 1	NM_178812.4:c.1381-1417_1… NM_178812.4:c.1381-1417_1381-1415del	N/A	Intron Variant
MTDH transcript variant X1	XM_011517368.3:c.1405-141… XM_011517368.3:c.1405-1417_1405-1415del	N/A	Intron Variant
MTDH transcript variant X2	XM_011517369.4:c.1470+386… XM_011517369.4:c.1470+3863_1470+3865del	N/A	Intron Variant
MTDH transcript variant X3	XM_011517370.4:c.1380+386… XM_011517370.4:c.1380+3863_1380+3865del	N/A	Intron Variant
MTDH transcript variant X5	XM_017013968.3:c.1281+386… XM_017013968.3:c.1281+3863_1281+3865del	N/A	Intron Variant
MTDH transcript variant X4	XM_047422418.1:c.1314+386… XM_047422418.1:c.1314+3863_1314+3865del	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	(C)₁₂=	delCCC	delCC	delC	dupC	dupCC
GRCh38.p14 chr 8	NC_000008.11:g.97717623_97717634=	NC_000008.11:g.97717632_97717634del	NC_000008.11:g.97717633_97717634del	NC_000008.11:g.97717634del	NC_000008.11:g.97717634dup	NC_000008.11:g.97717633_97717634dup
GRCh37.p13 chr 8	NC_000008.10:g.98729851_98729862=	NC_000008.10:g.98729860_98729862del	NC_000008.10:g.98729861_98729862del	NC_000008.10:g.98729862del	NC_000008.10:g.98729862dup	NC_000008.10:g.98729861_98729862dup
MTDH transcript variant 2	NM_001363136.1:c.1315-1426=	NM_001363136.1:c.1315-1417_1315-1415del	NM_001363136.1:c.1315-1416_1315-1415del	NM_001363136.1:c.1315-1415del	NM_001363136.1:c.1315-1415dup	NM_001363136.1:c.1315-1416_1315-1415dup
MTDH transcript variant 3	NM_001363137.1:c.1471-1426=	NM_001363137.1:c.1471-1417_1471-1415del	NM_001363137.1:c.1471-1416_1471-1415del	NM_001363137.1:c.1471-1415del	NM_001363137.1:c.1471-1415dup	NM_001363137.1:c.1471-1416_1471-1415dup
MTDH transcript variant 4	NM_001363138.1:c.1282-1426=	NM_001363138.1:c.1282-1417_1282-1415del	NM_001363138.1:c.1282-1416_1282-1415del	NM_001363138.1:c.1282-1415del	NM_001363138.1:c.1282-1415dup	NM_001363138.1:c.1282-1416_1282-1415dup
MTDH transcript variant 5	NM_001363139.1:c.1216-1426=	NM_001363139.1:c.1216-1417_1216-1415del	NM_001363139.1:c.1216-1416_1216-1415del	NM_001363139.1:c.1216-1415del	NM_001363139.1:c.1216-1415dup	NM_001363139.1:c.1216-1416_1216-1415dup
MTDH transcript	NM_178812.3:c.1381-1426=	NM_178812.3:c.1381-1417_1381-1415del	NM_178812.3:c.1381-1416_1381-1415del	NM_178812.3:c.1381-1415del	NM_178812.3:c.1381-1415dup	NM_178812.3:c.1381-1416_1381-1415dup
MTDH transcript variant 1	NM_178812.4:c.1381-1426=	NM_178812.4:c.1381-1417_1381-1415del	NM_178812.4:c.1381-1416_1381-1415del	NM_178812.4:c.1381-1415del	NM_178812.4:c.1381-1415dup	NM_178812.4:c.1381-1416_1381-1415dup
MTDH transcript variant X1	XM_005251098.1:c.1315-1426=	XM_005251098.1:c.1315-1417_1315-1415del	XM_005251098.1:c.1315-1416_1315-1415del	XM_005251098.1:c.1315-1415del	XM_005251098.1:c.1315-1415dup	XM_005251098.1:c.1315-1416_1315-1415dup
MTDH transcript variant X2	XM_005251099.1:c.1282-1426=	XM_005251099.1:c.1282-1417_1282-1415del	XM_005251099.1:c.1282-1416_1282-1415del	XM_005251099.1:c.1282-1415del	XM_005251099.1:c.1282-1415dup	XM_005251099.1:c.1282-1416_1282-1415dup
MTDH transcript variant X1	XM_011517368.3:c.1405-1426=	XM_011517368.3:c.1405-1417_1405-1415del	XM_011517368.3:c.1405-1416_1405-1415del	XM_011517368.3:c.1405-1415del	XM_011517368.3:c.1405-1415dup	XM_011517368.3:c.1405-1416_1405-1415dup
MTDH transcript variant X2	XM_011517369.4:c.1470+3854=	XM_011517369.4:c.1470+3863_1470+3865del	XM_011517369.4:c.1470+3864_1470+3865del	XM_011517369.4:c.1470+3865del	XM_011517369.4:c.1470+3865dup	XM_011517369.4:c.1470+3864_1470+3865dup
MTDH transcript variant X3	XM_011517370.4:c.1380+3854=	XM_011517370.4:c.1380+3863_1380+3865del	XM_011517370.4:c.1380+3864_1380+3865del	XM_011517370.4:c.1380+3865del	XM_011517370.4:c.1380+3865dup	XM_011517370.4:c.1380+3864_1380+3865dup
MTDH transcript variant X5	XM_017013968.3:c.1281+3854=	XM_017013968.3:c.1281+3863_1281+3865del	XM_017013968.3:c.1281+3864_1281+3865del	XM_017013968.3:c.1281+3865del	XM_017013968.3:c.1281+3865dup	XM_017013968.3:c.1281+3864_1281+3865dup
MTDH transcript variant X4	XM_047422418.1:c.1314+3854=	XM_047422418.1:c.1314+3863_1314+3865del	XM_047422418.1:c.1314+3864_1314+3865del	XM_047422418.1:c.1314+3865del	XM_047422418.1:c.1314+3865dup	XM_047422418.1:c.1314+3864_1314+3865dup

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#.

41 SubSNP, 16 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss43293041	Mar 14, 2006 (126)
2	HGSV	ss79856557	Dec 15, 2007 (129)
3	HGSV	ss83301120	Dec 15, 2007 (129)
4	BCMHGSC_JDW	ss103772539	Mar 15, 2016 (147)
5	GMI	ss288924166	May 04, 2012 (137)
6	PJP	ss295392867	May 09, 2011 (134)
7	SSMP	ss663883467	Apr 01, 2015 (144)
8	EVA_GENOME_DK	ss1577253470	Apr 01, 2015 (144)
9	JJLAB	ss2030926807	Sep 14, 2016 (149)
10	SYSTEMSBIOZJU	ss2627107176	Nov 08, 2017 (151)
11	SWEGEN	ss3003673895	Nov 08, 2017 (151)
12	MCHAISSO	ss3065198953	Nov 08, 2017 (151)
13	MCHAISSO	ss3066216536	Nov 08, 2017 (151)
14	BEROUKHIMLAB	ss3644267221	Oct 12, 2018 (152)
15	EVA_DECODE	ss3722610711	Jul 13, 2019 (153)
16	EVA_DECODE	ss3722610712	Jul 13, 2019 (153)
17	EVA_DECODE	ss3722610713	Jul 13, 2019 (153)
18	ACPOP	ss3735926014	Jul 13, 2019 (153)
19	ACPOP	ss3735926015	Jul 13, 2019 (153)
20	EVA	ss3831311814	Apr 26, 2020 (154)
21	EVA	ss3844623598	Apr 26, 2020 (154)
22	GNOMAD	ss4189843127	Apr 26, 2021 (155)
23	GNOMAD	ss4189843128	Apr 26, 2021 (155)
24	GNOMAD	ss4189843129	Apr 26, 2021 (155)
25	GNOMAD	ss4189843130	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5190082052	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5190082053	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5190082054	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5190082055	Apr 26, 2021 (155)
30	1000G_HIGH_COVERAGE	ss5278227472	Oct 16, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5278227473	Oct 16, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5278227474	Oct 16, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5278227475	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5474676808	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5474676809	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5474676810	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5732545854	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5732545855	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5732545856	Oct 16, 2022 (156)
40	EVA	ss5830947929	Oct 16, 2022 (156)
41	EVA	ss5856491179	Oct 16, 2022 (156)
42	The Danish reference pan genome	NC_000008.10 - 98729851	Apr 26, 2020 (154)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305144804 (NC_000008.11:97717622::C 4033/122264) Row 305144805 (NC_000008.11:97717622::CC 23/122412) Row 305144806 (NC_000008.11:97717622:C: 48060/122086)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305144804 (NC_000008.11:97717622::C 4033/122264) Row 305144805 (NC_000008.11:97717622::CC 23/122412) Row 305144806 (NC_000008.11:97717622:C: 48060/122086)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305144804 (NC_000008.11:97717622::C 4033/122264) Row 305144805 (NC_000008.11:97717622::CC 23/122412) Row 305144806 (NC_000008.11:97717622:C: 48060/122086)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305144804 (NC_000008.11:97717622::C 4033/122264) Row 305144805 (NC_000008.11:97717622::CC 23/122412) Row 305144806 (NC_000008.11:97717622:C: 48060/122086)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305144804 (NC_000008.11:97717622::C 4033/122264) Row 305144805 (NC_000008.11:97717622::CC 23/122412) Row 305144806 (NC_000008.11:97717622:C: 48060/122086)...	-	Apr 26, 2021 (155)
48	Northern Sweden Submission ignored due to conflicting rows: Row 9210879 (NC_000008.10:98729850:C: 173/598) Row 9210880 (NC_000008.10:98729850::C 18/598)	-	Jul 13, 2019 (153)
49	Northern Sweden Submission ignored due to conflicting rows: Row 9210879 (NC_000008.10:98729850:C: 173/598) Row 9210880 (NC_000008.10:98729850::C 18/598)	-	Jul 13, 2019 (153)
50	8.3KJPN Submission ignored due to conflicting rows: Row 48051359 (NC_000008.10:98729850:C: 10613/16744) Row 48051360 (NC_000008.10:98729850:CC: 55/16744) Row 48051361 (NC_000008.10:98729850::C 165/16744)...	-	Apr 26, 2021 (155)
51	8.3KJPN Submission ignored due to conflicting rows: Row 48051359 (NC_000008.10:98729850:C: 10613/16744) Row 48051360 (NC_000008.10:98729850:CC: 55/16744) Row 48051361 (NC_000008.10:98729850::C 165/16744)...	-	Apr 26, 2021 (155)
52	8.3KJPN Submission ignored due to conflicting rows: Row 48051359 (NC_000008.10:98729850:C: 10613/16744) Row 48051360 (NC_000008.10:98729850:CC: 55/16744) Row 48051361 (NC_000008.10:98729850::C 165/16744)...	-	Apr 26, 2021 (155)
53	8.3KJPN Submission ignored due to conflicting rows: Row 48051359 (NC_000008.10:98729850:C: 10613/16744) Row 48051360 (NC_000008.10:98729850:CC: 55/16744) Row 48051361 (NC_000008.10:98729850::C 165/16744)...	-	Apr 26, 2021 (155)
54	14KJPN Submission ignored due to conflicting rows: Row 66382958 (NC_000008.11:97717622:C: 17949/28256) Row 66382959 (NC_000008.11:97717622:CC: 61/28256) Row 66382960 (NC_000008.11:97717622::C 282/28256)	-	Oct 16, 2022 (156)
55	14KJPN Submission ignored due to conflicting rows: Row 66382958 (NC_000008.11:97717622:C: 17949/28256) Row 66382959 (NC_000008.11:97717622:CC: 61/28256) Row 66382960 (NC_000008.11:97717622::C 282/28256)	-	Oct 16, 2022 (156)
56	14KJPN Submission ignored due to conflicting rows: Row 66382958 (NC_000008.11:97717622:C: 17949/28256) Row 66382959 (NC_000008.11:97717622:CC: 61/28256) Row 66382960 (NC_000008.11:97717622::C 282/28256)	-	Oct 16, 2022 (156)
57	ALFA	NC_000008.11 - 97717623	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)
rs74218441	Oct 15, 2011 (136)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4189843130, ss5278227474	NC_000008.11:97717622:CCC:	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCC	(self)
2861684628	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCC	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCC	(self)
ss5190082053	NC_000008.10:98729850:CC:	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCC	(self)
ss3722610713, ss4189843129, ss5278227475, ss5474676809, ss5732545855	NC_000008.11:97717622:CC:	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCC	(self)
2861684628	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCC	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCC	(self)
ss103772539	NT_008046.16:12003409:CC:	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCC	(self)
ss288924166, ss295392867	NC_000008.9:98799026:C:	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
ss79856557, ss83301120	NC_000008.9:98799037:C:	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
1238309, ss663883467, ss1577253470, ss2030926807, ss2627107176, ss3003673895, ss3644267221, ss3735926014, ss3831311814, ss5190082052, ss5830947929	NC_000008.10:98729850:C:	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
ss3065198953, ss3066216536, ss3844623598, ss5278227472, ss5474676808, ss5732545854, ss5856491179	NC_000008.11:97717622:C:	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
2861684628	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCCC	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
ss3722610712	NC_000008.11:97717623:C:	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
ss43293041	NT_008046.16:12003399:C:	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
ss3735926015, ss5190082054	NC_000008.10:98729850::C	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss4189843127, ss5278227473, ss5474676810, ss5732545856	NC_000008.11:97717622::C	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
2861684628	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCCCCC	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss3722610711	NC_000008.11:97717624::C	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss5190082055	NC_000008.10:98729850::CC	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
ss4189843128	NC_000008.11:97717622::CC	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
2861684628	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCCCCCC	NC_000008.11:97717622:CCCCCCCCCCCC… NC_000008.11:97717622:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(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 rs35043860

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

rs35043860