Name: rs35085113
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.

rs35085113

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:36184250-36184261 (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 / dupCCC / dup(C)₄
Variation Type: Indel Insertion and Deletion
Frequency: delCCC=0.0000 (0/2250, ALFA)
delCC=0.0000 (0/2250, ALFA)
delC=0.0000 (0/2250, ALFA) (+ 4 more)
dupC=0.0000 (0/2250, ALFA)
dupCC=0.0000 (0/2250, ALFA)
dupCCC=0.0000 (0/2250, ALFA)
dup(C)₄=0.0000 (0/2250, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: BRPF3-AS1 : 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	HWEP
Total	Global	2250	CCCCCCCCCCCC=1.0000	CCCCCCCCC=0.0000, CCCCCCCCCC=0.0000, CCCCCCCCCCC=0.0000, CCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCCCC=0.0000	1.0	N/A
European	Sub	1366	CCCCCCCCCCCC=1.0000	CCCCCCCCC=0.0000, CCCCCCCCCC=0.0000, CCCCCCCCCCC=0.0000, CCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCCCC=0.0000	1.0	N/A
African	Sub	542	CCCCCCCCCCCC=1.000	CCCCCCCCC=0.000, CCCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCCCC=0.000	1.0	N/A
African Others	Sub	38	CCCCCCCCCCCC=1.00	CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCCC=0.00	1.0	N/A
African American	Sub	504	CCCCCCCCCCCC=1.000	CCCCCCCCC=0.000, CCCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCCCC=0.000	1.0	N/A
Asian	Sub	38	CCCCCCCCCCCC=1.00	CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCCC=0.00	1.0	N/A
East Asian	Sub	34	CCCCCCCCCCCC=1.00	CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCCC=0.00	1.0	N/A
Other Asian	Sub	4	CCCCCCCCCCCC=1.0	CCCCCCCCC=0.0, CCCCCCCCCC=0.0, CCCCCCCCCCC=0.0, CCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCCCC=0.0	1.0	N/A
Latin American 1	Sub	26	CCCCCCCCCCCC=1.00	CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCCC=0.00	1.0	N/A
Latin American 2	Sub	182	CCCCCCCCCCCC=1.000	CCCCCCCCC=0.000, CCCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCCCC=0.000	1.0	N/A
South Asian	Sub	8	CCCCCCCCCCCC=1.0	CCCCCCCCC=0.0, CCCCCCCCCC=0.0, CCCCCCCCCCC=0.0, CCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCCCC=0.0	1.0	N/A
Other	Sub	88	CCCCCCCCCCCC=1.00	CCCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCCC=0.00	1.0	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	2250	(C)₁₂=1.0000	delCCC=0.0000, delCC=0.0000, delC=0.0000, dupC=0.0000, dupCC=0.0000, dupCCC=0.0000, dup(C)₄=0.0000
Allele Frequency Aggregator	European	Sub	1366	(C)₁₂=1.0000	delCCC=0.0000, delCC=0.0000, delC=0.0000, dupC=0.0000, dupCC=0.0000, dupCCC=0.0000, dup(C)₄=0.0000
Allele Frequency Aggregator	African	Sub	542	(C)₁₂=1.000	delCCC=0.000, delCC=0.000, delC=0.000, dupC=0.000, dupCC=0.000, dupCCC=0.000, dup(C)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	182	(C)₁₂=1.000	delCCC=0.000, delCC=0.000, delC=0.000, dupC=0.000, dupCC=0.000, dupCCC=0.000, dup(C)₄=0.000
Allele Frequency Aggregator	Other	Sub	88	(C)₁₂=1.00	delCCC=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00, dup(C)₄=0.00
Allele Frequency Aggregator	Asian	Sub	38	(C)₁₂=1.00	delCCC=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00, dup(C)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	26	(C)₁₂=1.00	delCCC=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00, dup(C)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	8	(C)₁₂=1.0	delCCC=0.0, delCC=0.0, delC=0.0, dupC=0.0, dupCC=0.0, dupCCC=0.0, dup(C)₄=0.0

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 6	NC_000006.12:g.36184259_36184261del
GRCh38.p14 chr 6	NC_000006.12:g.36184260_36184261del
GRCh38.p14 chr 6	NC_000006.12:g.36184261del
GRCh38.p14 chr 6	NC_000006.12:g.36184261dup
GRCh38.p14 chr 6	NC_000006.12:g.36184260_36184261dup
GRCh38.p14 chr 6	NC_000006.12:g.36184259_36184261dup
GRCh38.p14 chr 6	NC_000006.12:g.36184258_36184261dup
GRCh37.p13 chr 6	NC_000006.11:g.36152036_36152038del
GRCh37.p13 chr 6	NC_000006.11:g.36152037_36152038del
GRCh37.p13 chr 6	NC_000006.11:g.36152038del
GRCh37.p13 chr 6	NC_000006.11:g.36152038dup
GRCh37.p13 chr 6	NC_000006.11:g.36152037_36152038dup
GRCh37.p13 chr 6	NC_000006.11:g.36152036_36152038dup
GRCh37.p13 chr 6	NC_000006.11:g.36152035_36152038dup

Gene: BRPF3-AS1, uncharacterized BRPF3-AS1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
BRPF3-AS1 transcript variant X6	XR_001744105.2:n.	N/A	Intron Variant
BRPF3-AS1 transcript variant X1	XR_427918.4:n.	N/A	Intron Variant
BRPF3-AS1 transcript variant X2	XR_926750.3:n.	N/A	Intron Variant
BRPF3-AS1 transcript variant X3	XR_926752.3:n.	N/A	Intron Variant
BRPF3-AS1 transcript variant X4	XR_926753.3:n.	N/A	Intron Variant
BRPF3-AS1 transcript variant X5	XR_926754.2:n.	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	dupCCC	dup(C)₄
GRCh38.p14 chr 6	NC_000006.12:g.36184250_36184261=	NC_000006.12:g.36184259_36184261del	NC_000006.12:g.36184260_36184261del	NC_000006.12:g.36184261del	NC_000006.12:g.36184261dup	NC_000006.12:g.36184260_36184261dup	NC_000006.12:g.36184259_36184261dup	NC_000006.12:g.36184258_36184261dup
GRCh37.p13 chr 6	NC_000006.11:g.36152027_36152038=	NC_000006.11:g.36152036_36152038del	NC_000006.11:g.36152037_36152038del	NC_000006.11:g.36152038del	NC_000006.11:g.36152038dup	NC_000006.11:g.36152037_36152038dup	NC_000006.11:g.36152036_36152038dup	NC_000006.11:g.36152035_36152038dup

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#.

44 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42704519	Mar 14, 2006 (126)
2	HUMANGENOME_JCVI	ss95425691	Feb 13, 2009 (130)
3	PJP	ss295275253	May 31, 2013 (138)
4	TISHKOFF	ss554268421	Apr 25, 2013 (138)
5	TISHKOFF	ss554268423	Apr 25, 2013 (138)
6	BILGI_BIOE	ss666350750	Apr 25, 2013 (138)
7	EVA_UK10K_ALSPAC	ss1705121273	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1705121696	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1710264537	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1710264542	Apr 01, 2015 (144)
11	HAMMER_LAB	ss1804381027	Sep 08, 2015 (146)
12	PACBIO	ss3785445834	Jul 13, 2019 (153)
13	PACBIO	ss3785445835	Jul 13, 2019 (153)
14	PACBIO	ss3790801572	Jul 13, 2019 (153)
15	PACBIO	ss3790801573	Jul 13, 2019 (153)
16	PACBIO	ss3795680199	Jul 13, 2019 (153)
17	PACBIO	ss3795680200	Jul 13, 2019 (153)
18	EVA	ss3829868089	Apr 26, 2020 (154)
19	GNOMAD	ss4139907589	Apr 26, 2021 (155)
20	GNOMAD	ss4139907592	Apr 26, 2021 (155)
21	GNOMAD	ss4139907593	Apr 26, 2021 (155)
22	GNOMAD	ss4139907594	Apr 26, 2021 (155)
23	GNOMAD	ss4139907597	Apr 26, 2021 (155)
24	GNOMAD	ss4139907598	Apr 26, 2021 (155)
25	GNOMAD	ss4139907599	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5177026996	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5177026997	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5177026998	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5177026999	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5177027000	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5177027001	Apr 26, 2021 (155)
32	HUGCELL_USP	ss5465777094	Oct 13, 2022 (156)
33	HUGCELL_USP	ss5465777095	Oct 13, 2022 (156)
34	HUGCELL_USP	ss5465777096	Oct 13, 2022 (156)
35	HUGCELL_USP	ss5465777098	Oct 13, 2022 (156)
36	TOMMO_GENOMICS	ss5714933500	Oct 13, 2022 (156)
37	TOMMO_GENOMICS	ss5714933501	Oct 13, 2022 (156)
38	TOMMO_GENOMICS	ss5714933502	Oct 13, 2022 (156)
39	TOMMO_GENOMICS	ss5714933503	Oct 13, 2022 (156)
40	TOMMO_GENOMICS	ss5714933504	Oct 13, 2022 (156)
41	TOMMO_GENOMICS	ss5714933505	Oct 13, 2022 (156)
42	EVA	ss5842092426	Oct 13, 2022 (156)
43	EVA	ss5842092427	Oct 13, 2022 (156)
44	EVA	ss5842092428	Oct 13, 2022 (156)
45	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 17544583 (NC_000006.11:36152026::CC 2427/3854) Row 17544584 (NC_000006.11:36152026:C: 782/3854)	-	Oct 12, 2018 (152)
46	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 17544583 (NC_000006.11:36152026::CC 2427/3854) Row 17544584 (NC_000006.11:36152026:C: 782/3854)	-	Oct 12, 2018 (152)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222122905 (NC_000006.12:36184249::C 12682/89410) Row 222122908 (NC_000006.12:36184249::CC 21606/88990) Row 222122909 (NC_000006.12:36184249::CCC 1074/89736)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222122905 (NC_000006.12:36184249::C 12682/89410) Row 222122908 (NC_000006.12:36184249::CC 21606/88990) Row 222122909 (NC_000006.12:36184249::CCC 1074/89736)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222122905 (NC_000006.12:36184249::C 12682/89410) Row 222122908 (NC_000006.12:36184249::CC 21606/88990) Row 222122909 (NC_000006.12:36184249::CCC 1074/89736)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222122905 (NC_000006.12:36184249::C 12682/89410) Row 222122908 (NC_000006.12:36184249::CC 21606/88990) Row 222122909 (NC_000006.12:36184249::CCC 1074/89736)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222122905 (NC_000006.12:36184249::C 12682/89410) Row 222122908 (NC_000006.12:36184249::CC 21606/88990) Row 222122909 (NC_000006.12:36184249::CCC 1074/89736)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222122905 (NC_000006.12:36184249::C 12682/89410) Row 222122908 (NC_000006.12:36184249::CC 21606/88990) Row 222122909 (NC_000006.12:36184249::CCC 1074/89736)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222122905 (NC_000006.12:36184249::C 12682/89410) Row 222122908 (NC_000006.12:36184249::CC 21606/88990) Row 222122909 (NC_000006.12:36184249::CCC 1074/89736)...	-	Apr 26, 2021 (155)
54	8.3KJPN Submission ignored due to conflicting rows: Row 34996303 (NC_000006.11:36152026:C: 2679/13616) Row 34996304 (NC_000006.11:36152026::C 1564/13616) Row 34996305 (NC_000006.11:36152026::CC 1195/13616)...	-	Apr 26, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 34996303 (NC_000006.11:36152026:C: 2679/13616) Row 34996304 (NC_000006.11:36152026::C 1564/13616) Row 34996305 (NC_000006.11:36152026::CC 1195/13616)...	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 34996303 (NC_000006.11:36152026:C: 2679/13616) Row 34996304 (NC_000006.11:36152026::C 1564/13616) Row 34996305 (NC_000006.11:36152026::CC 1195/13616)...	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 34996303 (NC_000006.11:36152026:C: 2679/13616) Row 34996304 (NC_000006.11:36152026::C 1564/13616) Row 34996305 (NC_000006.11:36152026::CC 1195/13616)...	-	Apr 26, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 34996303 (NC_000006.11:36152026:C: 2679/13616) Row 34996304 (NC_000006.11:36152026::C 1564/13616) Row 34996305 (NC_000006.11:36152026::CC 1195/13616)...	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 34996303 (NC_000006.11:36152026:C: 2679/13616) Row 34996304 (NC_000006.11:36152026::C 1564/13616) Row 34996305 (NC_000006.11:36152026::CC 1195/13616)...	-	Apr 26, 2021 (155)
60	14KJPN Submission ignored due to conflicting rows: Row 48770604 (NC_000006.12:36184249:C: 4417/28208) Row 48770605 (NC_000006.12:36184249::CC 2474/28208) Row 48770606 (NC_000006.12:36184249::C 2740/28208)...	-	Oct 13, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 48770604 (NC_000006.12:36184249:C: 4417/28208) Row 48770605 (NC_000006.12:36184249::CC 2474/28208) Row 48770606 (NC_000006.12:36184249::C 2740/28208)...	-	Oct 13, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 48770604 (NC_000006.12:36184249:C: 4417/28208) Row 48770605 (NC_000006.12:36184249::CC 2474/28208) Row 48770606 (NC_000006.12:36184249::C 2740/28208)...	-	Oct 13, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 48770604 (NC_000006.12:36184249:C: 4417/28208) Row 48770605 (NC_000006.12:36184249::CC 2474/28208) Row 48770606 (NC_000006.12:36184249::C 2740/28208)...	-	Oct 13, 2022 (156)
64	14KJPN Submission ignored due to conflicting rows: Row 48770604 (NC_000006.12:36184249:C: 4417/28208) Row 48770605 (NC_000006.12:36184249::CC 2474/28208) Row 48770606 (NC_000006.12:36184249::C 2740/28208)...	-	Oct 13, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 48770604 (NC_000006.12:36184249:C: 4417/28208) Row 48770605 (NC_000006.12:36184249::CC 2474/28208) Row 48770606 (NC_000006.12:36184249::C 2740/28208)...	-	Oct 13, 2022 (156)
66	UK 10K study - Twins Submission ignored due to conflicting rows: Row 17544583 (NC_000006.11:36152026::CC 2310/3708) Row 17544584 (NC_000006.11:36152026:C: 751/3708)	-	Oct 12, 2018 (152)
67	UK 10K study - Twins Submission ignored due to conflicting rows: Row 17544583 (NC_000006.11:36152026::CC 2310/3708) Row 17544584 (NC_000006.11:36152026:C: 751/3708)	-	Oct 12, 2018 (152)
68	ALFA	NC_000006.12 - 36184250	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)
rs370256820	May 15, 2013 (138)
rs898563854	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4139907599	NC_000006.12:36184249:CCC:	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCC	(self)
13343793875	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCC	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCC	(self)
ss5177026999	NC_000006.11:36152026:CC:	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCC	(self)
ss554268421	NC_000006.11:36152036:CC:	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCC	(self)
ss4139907598, ss5465777098, ss5714933503	NC_000006.12:36184249:CC:	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCC	(self)
13343793875	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCC	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCC	(self)
ss666350750, ss1705121273, ss1705121696, ss3785445834, ss3790801572, ss3795680199, ss5177026996, ss5842092426	NC_000006.11:36152026:C:	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
ss554268423	NC_000006.11:36152037:C:	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
ss4139907597, ss5465777095, ss5714933500	NC_000006.12:36184249:C:	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
13343793875	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCC	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
ss1804381027, ss5177026997, ss5842092428	NC_000006.11:36152026::C	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss4139907589, ss5465777096, ss5714933502	NC_000006.12:36184249::C	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
13343793875	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCC	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss295275253	NC_000006.10:36260005::CC	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
ss3785445835, ss3790801573, ss3795680200, ss3829868089, ss5177026998, ss5842092427	NC_000006.11:36152026::CC	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
ss1710264537, ss1710264542	NC_000006.11:36152027::CC	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
ss4139907592, ss5465777094, ss5714933501	NC_000006.12:36184249::CC	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
13343793875	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCCC	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
ss42704519	NT_007592.15:36092026::CC	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
ss95425691	NT_007592.15:36092038::CC	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
ss5177027000	NC_000006.11:36152026::CCC	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCCCC	(self)
ss4139907593, ss5714933504	NC_000006.12:36184249::CCC	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCCCC	(self)
13343793875	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCCCC	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCCCC	(self)
ss5177027001	NC_000006.11:36152026::CCCC	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCCCCC	(self)
ss4139907594, ss5714933505	NC_000006.12:36184249::CCCC	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCCCCC	(self)
13343793875	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCCCCC	NC_000006.12:36184249:CCCCCCCCCCCC… NC_000006.12:36184249:CCCCCCCCCCCC:CCCCCCCCCCCCCCCC	(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 rs35085113

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

rs35085113