Name: rs71260899
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.

rs71260899

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:64722744-64722756 (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: del(G)₈ / del(G)₇ / delGGG / delGG…
del(G)₈ / del(G)₇ / delGGG / delGG / delG / dupG / dupGG / dupGGG / dup(G)₄
Variation Type: Indel Insertion and Deletion
Frequency: del(G)₈=0.0000 (0/4084, ALFA)
del(G)₇=0.0000 (0/4084, ALFA)
delGGG=0.0000 (0/4084, ALFA) (+ 6 more)
delGG=0.0000 (0/4084, ALFA)
delG=0.0000 (0/4084, ALFA)
dupG=0.0000 (0/4084, ALFA)
dupGG=0.0000 (0/4084, ALFA)
dupGGG=0.0000 (0/4084, ALFA)
dupG=0.052 (18/344, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CYP7B1 : 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	4084	GGGGGGGGGGGGG=1.0000	GGGGG=0.0000, GGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGG=0.0000	1.0	N/A
European	Sub	1690	GGGGGGGGGGGGG=1.0000	GGGGG=0.0000, GGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGG=0.0000	1.0	N/A
African	Sub	2006	GGGGGGGGGGGGG=1.0000	GGGGG=0.0000, GGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGG=0.0000	1.0	N/A
African Others	Sub	84	GGGGGGGGGGGGG=1.00	GGGGG=0.00, GGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00	1.0	N/A
African American	Sub	1922	GGGGGGGGGGGGG=1.0000	GGGGG=0.0000, GGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGG=0.0000	1.0	N/A
Asian	Sub	10	GGGGGGGGGGGGG=1.0	GGGGG=0.0, GGGGGG=0.0, GGGGGGGGGG=0.0, GGGGGGGGGGG=0.0, GGGGGGGGGGGG=0.0, GGGGGGGGGGGGGG=0.0, GGGGGGGGGGGGGGG=0.0, GGGGGGGGGGGGGGGG=0.0	1.0	N/A
East Asian	Sub	6	GGGGGGGGGGGGG=1.0	GGGGG=0.0, GGGGGG=0.0, GGGGGGGGGG=0.0, GGGGGGGGGGG=0.0, GGGGGGGGGGGG=0.0, GGGGGGGGGGGGGG=0.0, GGGGGGGGGGGGGGG=0.0, GGGGGGGGGGGGGGGG=0.0	1.0	N/A
Other Asian	Sub	4	GGGGGGGGGGGGG=1.0	GGGGG=0.0, GGGGGG=0.0, GGGGGGGGGG=0.0, GGGGGGGGGGG=0.0, GGGGGGGGGGGG=0.0, GGGGGGGGGGGGGG=0.0, GGGGGGGGGGGGGGG=0.0, GGGGGGGGGGGGGGGG=0.0	1.0	N/A
Latin American 1	Sub	64	GGGGGGGGGGGGG=1.00	GGGGG=0.00, GGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00	1.0	N/A
Latin American 2	Sub	140	GGGGGGGGGGGGG=1.000	GGGGG=0.000, GGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000	1.0	N/A
South Asian	Sub	22	GGGGGGGGGGGGG=1.00	GGGGG=0.00, GGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00	1.0	N/A
Other	Sub	152	GGGGGGGGGGGGG=1.000	GGGGG=0.000, GGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	4084	(G)₁₃=1.0000	del(G)₈=0.0000, del(G)₇=0.0000, delGGG=0.0000, delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000
Allele Frequency Aggregator	African	Sub	2006	(G)₁₃=1.0000	del(G)₈=0.0000, del(G)₇=0.0000, delGGG=0.0000, delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000
Allele Frequency Aggregator	European	Sub	1690	(G)₁₃=1.0000	del(G)₈=0.0000, del(G)₇=0.0000, delGGG=0.0000, delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000
Allele Frequency Aggregator	Other	Sub	152	(G)₁₃=1.000	del(G)₈=0.000, del(G)₇=0.000, delGGG=0.000, delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000
Allele Frequency Aggregator	Latin American 2	Sub	140	(G)₁₃=1.000	del(G)₈=0.000, del(G)₇=0.000, delGGG=0.000, delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000
Allele Frequency Aggregator	Latin American 1	Sub	64	(G)₁₃=1.00	del(G)₈=0.00, del(G)₇=0.00, delGGG=0.00, delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00
Allele Frequency Aggregator	South Asian	Sub	22	(G)₁₃=1.00	del(G)₈=0.00, del(G)₇=0.00, delGGG=0.00, delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00
Allele Frequency Aggregator	Asian	Sub	10	(G)₁₃=1.0	del(G)₈=0.0, del(G)₇=0.0, delGGG=0.0, delGG=0.0, delG=0.0, dupG=0.0, dupGG=0.0, dupGGG=0.0
Northern Sweden	ACPOP	Study-wide	344	- No frequency provided	dupG=0.052

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.64722749_64722756del
GRCh38.p14 chr 8	NC_000008.11:g.64722750_64722756del
GRCh38.p14 chr 8	NC_000008.11:g.64722754_64722756del
GRCh38.p14 chr 8	NC_000008.11:g.64722755_64722756del
GRCh38.p14 chr 8	NC_000008.11:g.64722756del
GRCh38.p14 chr 8	NC_000008.11:g.64722756dup
GRCh38.p14 chr 8	NC_000008.11:g.64722755_64722756dup
GRCh38.p14 chr 8	NC_000008.11:g.64722754_64722756dup
GRCh38.p14 chr 8	NC_000008.11:g.64722753_64722756dup
GRCh37.p13 chr 8	NC_000008.10:g.65635306_65635313del
GRCh37.p13 chr 8	NC_000008.10:g.65635307_65635313del
GRCh37.p13 chr 8	NC_000008.10:g.65635311_65635313del
GRCh37.p13 chr 8	NC_000008.10:g.65635312_65635313del
GRCh37.p13 chr 8	NC_000008.10:g.65635313del
GRCh37.p13 chr 8	NC_000008.10:g.65635313dup
GRCh37.p13 chr 8	NC_000008.10:g.65635312_65635313dup
GRCh37.p13 chr 8	NC_000008.10:g.65635311_65635313dup
GRCh37.p13 chr 8	NC_000008.10:g.65635310_65635313dup
CYP7B1 RefSeqGene	NG_008338.2:g.81041_81048del
CYP7B1 RefSeqGene	NG_008338.2:g.81042_81048del
CYP7B1 RefSeqGene	NG_008338.2:g.81046_81048del
CYP7B1 RefSeqGene	NG_008338.2:g.81047_81048del
CYP7B1 RefSeqGene	NG_008338.2:g.81048del
CYP7B1 RefSeqGene	NG_008338.2:g.81048dup
CYP7B1 RefSeqGene	NG_008338.2:g.81047_81048dup
CYP7B1 RefSeqGene	NG_008338.2:g.81046_81048dup
CYP7B1 RefSeqGene	NG_008338.2:g.81045_81048dup

Gene: CYP7B1, cytochrome P450 family 7 subfamily B member 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CYP7B1 transcript variant 2	NM_001324112.2:c.122+7571… NM_001324112.2:c.122+75715_122+75722del	N/A	Intron Variant
CYP7B1 transcript variant 1	NM_004820.5:c.122+75715_1… NM_004820.5:c.122+75715_122+75722del	N/A	Intron Variant
CYP7B1 transcript variant X1	XM_017014002.2: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	(G)₁₃=	del(G)₈	del(G)₇	delGGG	delGG	delG	dupG	dupGG	dupGGG	dup(G)₄
GRCh38.p14 chr 8	NC_000008.11:g.64722744_64722756=	NC_000008.11:g.64722749_64722756del	NC_000008.11:g.64722750_64722756del	NC_000008.11:g.64722754_64722756del	NC_000008.11:g.64722755_64722756del	NC_000008.11:g.64722756del	NC_000008.11:g.64722756dup	NC_000008.11:g.64722755_64722756dup	NC_000008.11:g.64722754_64722756dup	NC_000008.11:g.64722753_64722756dup
GRCh37.p13 chr 8	NC_000008.10:g.65635301_65635313=	NC_000008.10:g.65635306_65635313del	NC_000008.10:g.65635307_65635313del	NC_000008.10:g.65635311_65635313del	NC_000008.10:g.65635312_65635313del	NC_000008.10:g.65635313del	NC_000008.10:g.65635313dup	NC_000008.10:g.65635312_65635313dup	NC_000008.10:g.65635311_65635313dup	NC_000008.10:g.65635310_65635313dup
CYP7B1 RefSeqGene	NG_008338.2:g.81036_81048=	NG_008338.2:g.81041_81048del	NG_008338.2:g.81042_81048del	NG_008338.2:g.81046_81048del	NG_008338.2:g.81047_81048del	NG_008338.2:g.81048del	NG_008338.2:g.81048dup	NG_008338.2:g.81047_81048dup	NG_008338.2:g.81046_81048dup	NG_008338.2:g.81045_81048dup
CYP7B1 transcript variant 2	NM_001324112.2:c.122+75722=	NM_001324112.2:c.122+75715_122+75722del	NM_001324112.2:c.122+75716_122+75722del	NM_001324112.2:c.122+75720_122+75722del	NM_001324112.2:c.122+75721_122+75722del	NM_001324112.2:c.122+75722del	NM_001324112.2:c.122+75722dup	NM_001324112.2:c.122+75721_122+75722dup	NM_001324112.2:c.122+75720_122+75722dup	NM_001324112.2:c.122+75719_122+75722dup
CYP7B1 transcript	NM_004820.3:c.122+75722=	NM_004820.3:c.122+75715_122+75722del	NM_004820.3:c.122+75716_122+75722del	NM_004820.3:c.122+75720_122+75722del	NM_004820.3:c.122+75721_122+75722del	NM_004820.3:c.122+75722del	NM_004820.3:c.122+75722dup	NM_004820.3:c.122+75721_122+75722dup	NM_004820.3:c.122+75720_122+75722dup	NM_004820.3:c.122+75719_122+75722dup
CYP7B1 transcript variant 1	NM_004820.5:c.122+75722=	NM_004820.5:c.122+75715_122+75722del	NM_004820.5:c.122+75716_122+75722del	NM_004820.5:c.122+75720_122+75722del	NM_004820.5:c.122+75721_122+75722del	NM_004820.5:c.122+75722del	NM_004820.5:c.122+75722dup	NM_004820.5:c.122+75721_122+75722dup	NM_004820.5:c.122+75720_122+75722dup	NM_004820.5:c.122+75719_122+75722dup

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#.

27 SubSNP, 14 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95494088	Oct 12, 2018 (152)
2	HUMANGENOME_JCVI	ss98027471	Mar 15, 2016 (147)
3	BCMHGSC_JDW	ss103769248	Mar 15, 2016 (147)
4	PJP	ss295384198	May 09, 2011 (137)
5	EVA_DECODE	ss3722175997	Jul 13, 2019 (153)
6	EVA_DECODE	ss3722175998	Jul 13, 2019 (153)
7	EVA_DECODE	ss3722175999	Jul 13, 2019 (153)
8	EVA_DECODE	ss3722176000	Jul 13, 2019 (153)
9	EVA_DECODE	ss3722176001	Jul 13, 2019 (153)
10	EVA_DECODE	ss3722176002	Jul 13, 2019 (153)
11	ACPOP	ss3735733432	Jul 13, 2019 (153)
12	PACBIO	ss3786166511	Jul 13, 2019 (153)
13	PACBIO	ss3791418734	Jul 13, 2019 (153)
14	PACBIO	ss3791418735	Jul 13, 2019 (153)
15	PACBIO	ss3796300100	Jul 13, 2019 (153)
16	PACBIO	ss3796300101	Jul 13, 2019 (153)
17	GNOMAD	ss4185846077	Apr 26, 2021 (155)
18	GNOMAD	ss4185846079	Apr 26, 2021 (155)
19	GNOMAD	ss4185846080	Apr 26, 2021 (155)
20	TOMMO_GENOMICS	ss5189079922	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5189079923	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5189079924	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5189079925	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5731252020	Oct 16, 2022 (156)
25	TOMMO_GENOMICS	ss5731252021	Oct 16, 2022 (156)
26	TOMMO_GENOMICS	ss5731252023	Oct 16, 2022 (156)
27	TOMMO_GENOMICS	ss5731252024	Oct 16, 2022 (156)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298461672 (NC_000008.11:64722743::GGGG 6/7416) Row 298461674 (NC_000008.11:64722743:G: 151/7396) Row 298461675 (NC_000008.11:64722743:GGG: 2/7416)...	-	Apr 26, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298461672 (NC_000008.11:64722743::GGGG 6/7416) Row 298461674 (NC_000008.11:64722743:G: 151/7396) Row 298461675 (NC_000008.11:64722743:GGG: 2/7416)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298461672 (NC_000008.11:64722743::GGGG 6/7416) Row 298461674 (NC_000008.11:64722743:G: 151/7396) Row 298461675 (NC_000008.11:64722743:GGG: 2/7416)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298461672 (NC_000008.11:64722743::GGGG 6/7416) Row 298461674 (NC_000008.11:64722743:G: 151/7396) Row 298461675 (NC_000008.11:64722743:GGG: 2/7416)...	-	Apr 26, 2021 (155)
32	Northern Sweden	NC_000008.10 - 65635301	Jul 13, 2019 (153)
33	8.3KJPN Submission ignored due to conflicting rows: Row 47049229 (NC_000008.10:65635300::GG 837/13308) Row 47049230 (NC_000008.10:65635300::GGG 359/13308) Row 47049231 (NC_000008.10:65635300::G 3906/13308)...	-	Apr 26, 2021 (155)
34	8.3KJPN Submission ignored due to conflicting rows: Row 47049229 (NC_000008.10:65635300::GG 837/13308) Row 47049230 (NC_000008.10:65635300::GGG 359/13308) Row 47049231 (NC_000008.10:65635300::G 3906/13308)...	-	Apr 26, 2021 (155)
35	8.3KJPN Submission ignored due to conflicting rows: Row 47049229 (NC_000008.10:65635300::GG 837/13308) Row 47049230 (NC_000008.10:65635300::GGG 359/13308) Row 47049231 (NC_000008.10:65635300::G 3906/13308)...	-	Apr 26, 2021 (155)
36	8.3KJPN Submission ignored due to conflicting rows: Row 47049229 (NC_000008.10:65635300::GG 837/13308) Row 47049230 (NC_000008.10:65635300::GGG 359/13308) Row 47049231 (NC_000008.10:65635300::G 3906/13308)...	-	Apr 26, 2021 (155)
37	14KJPN Submission ignored due to conflicting rows: Row 65089124 (NC_000008.11:64722743::GGG 419/25932) Row 65089125 (NC_000008.11:64722743::GG 1322/25932) Row 65089127 (NC_000008.11:64722743::G 7702/25932)...	-	Oct 16, 2022 (156)
38	14KJPN Submission ignored due to conflicting rows: Row 65089124 (NC_000008.11:64722743::GGG 419/25932) Row 65089125 (NC_000008.11:64722743::GG 1322/25932) Row 65089127 (NC_000008.11:64722743::G 7702/25932)...	-	Oct 16, 2022 (156)
39	14KJPN Submission ignored due to conflicting rows: Row 65089124 (NC_000008.11:64722743::GGG 419/25932) Row 65089125 (NC_000008.11:64722743::GG 1322/25932) Row 65089127 (NC_000008.11:64722743::G 7702/25932)...	-	Oct 16, 2022 (156)
40	14KJPN Submission ignored due to conflicting rows: Row 65089124 (NC_000008.11:64722743::GGG 419/25932) Row 65089125 (NC_000008.11:64722743::GG 1322/25932) Row 65089127 (NC_000008.11:64722743::G 7702/25932)...	-	Oct 16, 2022 (156)
41	ALFA	NC_000008.11 - 64722744	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)
rs149883482	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4185846080	NC_000008.11:64722743:GGGGGGGG:	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGG	(self)
2803128714	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGG	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGG	(self)
2803128714	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGG	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGG	(self)
ss4185846079	NC_000008.11:64722743:GGG:	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGG	(self)
2803128714	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGG	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGG	(self)
ss3722176002	NC_000008.11:64722743:GG:	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGG	(self)
2803128714	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGG	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGG	(self)
ss5189079925	NC_000008.10:65635300:G:	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGG	(self)
ss5731252024	NC_000008.11:64722743:G:	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGG	(self)
2803128714	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGG	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGG	(self)
ss3722176001	NC_000008.11:64722744:G:	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGG	(self)
ss103769248	NT_008183.19:17499703:G:	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGG	(self)
ss295384198	NC_000008.9:65797861::G	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
9018297, ss3735733432, ss3786166511, ss3791418734, ss3796300100, ss5189079924	NC_000008.10:65635300::G	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
ss5731252023	NC_000008.11:64722743::G	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
2803128714	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGG	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
ss3722176000	NC_000008.11:64722745::G	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
ss98027471	NT_008183.19:17499698:GGC:GGCG	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
ss95494088	NT_008183.19:17499714::G	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
ss3791418735, ss3796300101, ss5189079922	NC_000008.10:65635300::GG	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGGG	(self)
ss5731252021	NC_000008.11:64722743::GG	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGGG	(self)
2803128714	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGGG	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGGG	(self)
ss3722175999	NC_000008.11:64722745::GG	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGGG	(self)
ss5189079923	NC_000008.10:65635300::GGG	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGG	(self)
ss5731252020	NC_000008.11:64722743::GGG	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGG	(self)
2803128714	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGG	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGG	(self)
ss3722175998	NC_000008.11:64722745::GGG	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGG	(self)
ss4185846077	NC_000008.11:64722743::GGGG	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGG	(self)
ss3722175997	NC_000008.11:64722745::GGGG	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGG	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3564382760	NC_000008.11:64722743:GGGGGGG:	NC_000008.11:64722743:GGGGGGGGGGGG… NC_000008.11:64722743:GGGGGGGGGGGGG:GGGGGG

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

No publications for rs71260899

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
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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

rs71260899