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dbSNP Short Genetic Variations

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.

rs147936885

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr15:49962488 (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
A>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.006914 (1830/264690, TOPMED)
G=0.006353 (891/140252, GnomAD)
G=0.00642 (125/19468, ALFA) (+ 9 more)
G=0.0039 (25/6404, 1000G_30x)
G=0.0038 (19/5008, 1000G)
G=0.0036 (16/4480, Estonian)
G=0.0080 (31/3854, ALSPAC)
G=0.0070 (26/3708, TWINSUK)
G=0.012 (12/998, GoNL)
G=0.002 (1/600, NorthernSweden)
A=0.5 (2/4, SGDP_PRJ)
G=0.5 (2/4, SGDP_PRJ)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ATP8B4 : 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: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 19468 A=0.99358 G=0.00642
European Sub 14286 A=0.99265 G=0.00735
African Sub 3372 A=0.9967 G=0.0033
African Others Sub 114 A=1.000 G=0.000
African American Sub 3258 A=0.9966 G=0.0034
Asian Sub 112 A=1.000 G=0.000
East Asian Sub 86 A=1.00 G=0.00
Other Asian Sub 26 A=1.00 G=0.00
Latin American 1 Sub 146 A=0.993 G=0.007
Latin American 2 Sub 610 A=0.992 G=0.008
South Asian Sub 98 A=1.00 G=0.00
Other Sub 844 A=0.996 G=0.004


Help

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
TopMed Global Study-wide 264690 A=0.993086 G=0.006914
gnomAD - Genomes Global Study-wide 140252 A=0.993647 G=0.006353
gnomAD - Genomes European Sub 75940 A=0.99257 G=0.00743
gnomAD - Genomes African Sub 42054 A=0.99750 G=0.00250
gnomAD - Genomes American Sub 13650 A=0.98982 G=0.01018
gnomAD - Genomes Ashkenazi Jewish Sub 3324 A=0.9798 G=0.0202
gnomAD - Genomes East Asian Sub 3134 A=1.0000 G=0.0000
gnomAD - Genomes Other Sub 2150 A=0.9926 G=0.0074
Allele Frequency Aggregator Total Global 19468 A=0.99358 G=0.00642
Allele Frequency Aggregator European Sub 14286 A=0.99265 G=0.00735
Allele Frequency Aggregator African Sub 3372 A=0.9967 G=0.0033
Allele Frequency Aggregator Other Sub 844 A=0.996 G=0.004
Allele Frequency Aggregator Latin American 2 Sub 610 A=0.992 G=0.008
Allele Frequency Aggregator Latin American 1 Sub 146 A=0.993 G=0.007
Allele Frequency Aggregator Asian Sub 112 A=1.000 G=0.000
Allele Frequency Aggregator South Asian Sub 98 A=1.00 G=0.00
1000Genomes_30x Global Study-wide 6404 A=0.9961 G=0.0039
1000Genomes_30x African Sub 1786 A=0.9978 G=0.0022
1000Genomes_30x Europe Sub 1266 A=0.9874 G=0.0126
1000Genomes_30x South Asian Sub 1202 A=0.9975 G=0.0025
1000Genomes_30x East Asian Sub 1170 A=1.0000 G=0.0000
1000Genomes_30x American Sub 980 A=0.998 G=0.002
1000Genomes Global Study-wide 5008 A=0.9962 G=0.0038
1000Genomes African Sub 1322 A=0.9977 G=0.0023
1000Genomes East Asian Sub 1008 A=1.0000 G=0.0000
1000Genomes Europe Sub 1006 A=0.9891 G=0.0109
1000Genomes South Asian Sub 978 A=0.997 G=0.003
1000Genomes American Sub 694 A=0.997 G=0.003
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.9964 G=0.0036
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.9920 G=0.0080
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.9930 G=0.0070
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.988 G=0.012
Northern Sweden ACPOP Study-wide 600 A=0.998 G=0.002
SGDP_PRJ Global Study-wide 4 A=0.5 G=0.5
Help

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 15 NC_000015.10:g.49962488A>G
GRCh37.p13 chr 15 NC_000015.9:g.50254685A>G
Gene: ATP8B4, ATPase phospholipid transporting 8B4 (putative) (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ATP8B4 transcript variant 1 NM_024837.4:c.1244-468T>C N/A Intron Variant
ATP8B4 transcript variant 2 NR_073596.2:n. N/A Intron Variant
ATP8B4 transcript variant 3 NR_073597.2:n. N/A Intron Variant
ATP8B4 transcript variant 4 NR_073598.2:n. N/A Intron Variant
ATP8B4 transcript variant X1 XM_011522046.3:c.1439-468…

XM_011522046.3:c.1439-468T>C

N/A Intron Variant
ATP8B4 transcript variant X3 XM_011522047.3:c.1328-468…

XM_011522047.3:c.1328-468T>C

N/A Intron Variant
ATP8B4 transcript variant X6 XM_011522048.2:c.1328-468…

XM_011522048.2:c.1328-468T>C

N/A Intron Variant
ATP8B4 transcript variant X5 XM_011522049.3:c.1328-468…

XM_011522049.3:c.1328-468T>C

N/A Intron Variant
ATP8B4 transcript variant X7 XM_011522052.4:c.1328-468…

XM_011522052.4:c.1328-468T>C

N/A Intron Variant
ATP8B4 transcript variant X4 XM_011522053.2:c.1328-468…

XM_011522053.2:c.1328-468T>C

N/A Intron Variant
ATP8B4 transcript variant X21 XM_011522056.4:c.1328-468…

XM_011522056.4:c.1328-468T>C

N/A Intron Variant
ATP8B4 transcript variant X24 XM_011522058.4:c.1001-468…

XM_011522058.4:c.1001-468T>C

N/A Intron Variant
ATP8B4 transcript variant X25 XM_011522059.1:c.983-468T…

XM_011522059.1:c.983-468T>C

N/A Intron Variant
ATP8B4 transcript variant X26 XM_011522060.1:c.947-468T…

XM_011522060.1:c.947-468T>C

N/A Intron Variant
ATP8B4 transcript variant X27 XM_011522061.1:c.947-468T…

XM_011522061.1:c.947-468T>C

N/A Intron Variant
ATP8B4 transcript variant X28 XM_011522062.1:c.947-468T…

XM_011522062.1:c.947-468T>C

N/A Intron Variant
ATP8B4 transcript variant X29 XM_011522063.1:c.947-468T…

XM_011522063.1:c.947-468T>C

N/A Intron Variant
ATP8B4 transcript variant X38 XM_011522069.2:c.479-468T…

XM_011522069.2:c.479-468T>C

N/A Intron Variant
ATP8B4 transcript variant X13 XM_017022587.3:c.1244-468…

XM_017022587.3:c.1244-468T>C

N/A Intron Variant
ATP8B4 transcript variant X9 XM_017022591.2:c.1328-468…

XM_017022591.2:c.1328-468T>C

N/A Intron Variant
ATP8B4 transcript variant X23 XM_017022594.1:c.1001-468…

XM_017022594.1:c.1001-468T>C

N/A Intron Variant
ATP8B4 transcript variant X2 XM_024450065.2:c.1355-468…

XM_024450065.2:c.1355-468T>C

N/A Intron Variant
ATP8B4 transcript variant X10 XM_024450066.2:c.1280-468…

XM_024450066.2:c.1280-468T>C

N/A Intron Variant
ATP8B4 transcript variant X11 XM_024450067.2:c.1439-468…

XM_024450067.2:c.1439-468T>C

N/A Intron Variant
ATP8B4 transcript variant X32 XM_024450068.2:c.1439-468…

XM_024450068.2:c.1439-468T>C

N/A Intron Variant
ATP8B4 transcript variant X35 XM_024450069.1:c.692-468T…

XM_024450069.1:c.692-468T>C

N/A Intron Variant
ATP8B4 transcript variant X42 XM_024450070.2:c.1439-468…

XM_024450070.2:c.1439-468T>C

N/A Intron Variant
ATP8B4 transcript variant X8 XM_047433082.1:c.1328-468…

XM_047433082.1:c.1328-468T>C

N/A Intron Variant
ATP8B4 transcript variant X12 XM_047433083.1:c.1244-468…

XM_047433083.1:c.1244-468T>C

N/A Intron Variant
ATP8B4 transcript variant X14 XM_047433084.1:c.1226-468…

XM_047433084.1:c.1226-468T>C

N/A Intron Variant
ATP8B4 transcript variant X15 XM_047433085.1:c.1196-468…

XM_047433085.1:c.1196-468T>C

N/A Intron Variant
ATP8B4 transcript variant X16 XM_047433086.1:c.1355-468…

XM_047433086.1:c.1355-468T>C

N/A Intron Variant
ATP8B4 transcript variant X17 XM_047433087.1:c.1142-468…

XM_047433087.1:c.1142-468T>C

N/A Intron Variant
ATP8B4 transcript variant X18 XM_047433088.1:c.1115-468…

XM_047433088.1:c.1115-468T>C

N/A Intron Variant
ATP8B4 transcript variant X19 XM_047433089.1:c.1244-468…

XM_047433089.1:c.1244-468T>C

N/A Intron Variant
ATP8B4 transcript variant X20 XM_047433090.1:c.1031-468…

XM_047433090.1:c.1031-468T>C

N/A Intron Variant
ATP8B4 transcript variant X22 XM_047433091.1:c.1196-468…

XM_047433091.1:c.1196-468T>C

N/A Intron Variant
ATP8B4 transcript variant X30 XM_047433092.1:c.917-468T…

XM_047433092.1:c.917-468T>C

N/A Intron Variant
ATP8B4 transcript variant X31 XM_047433093.1:c.1085-468…

XM_047433093.1:c.1085-468T>C

N/A Intron Variant
ATP8B4 transcript variant X33 XM_047433094.1:c.1031-468…

XM_047433094.1:c.1031-468T>C

N/A Intron Variant
ATP8B4 transcript variant X34 XM_047433096.1:c.1031-468…

XM_047433096.1:c.1031-468T>C

N/A Intron Variant
ATP8B4 transcript variant X36 XM_047433097.1:c.611-468T…

XM_047433097.1:c.611-468T>C

N/A Intron Variant
ATP8B4 transcript variant X37 XM_047433098.1:c.611-468T…

XM_047433098.1:c.611-468T>C

N/A Intron Variant
ATP8B4 transcript variant X39 XM_047433099.1:c.1244-468…

XM_047433099.1:c.1244-468T>C

N/A Intron Variant
ATP8B4 transcript variant X40 XM_047433100.1:c.1439-468…

XM_047433100.1:c.1439-468T>C

N/A Intron Variant
ATP8B4 transcript variant X41 XM_011522070.2:c. N/A Genic Upstream Transcript Variant
ATP8B4 transcript variant X43 XR_002957687.2:n. N/A Intron Variant
Help

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
Help

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= G
GRCh38.p14 chr 15 NC_000015.10:g.49962488= NC_000015.10:g.49962488A>G
GRCh37.p13 chr 15 NC_000015.9:g.50254685= NC_000015.9:g.50254685A>G
ATP8B4 transcript variant 1 NM_024837.3:c.1244-468= NM_024837.3:c.1244-468T>C
ATP8B4 transcript variant 1 NM_024837.4:c.1244-468= NM_024837.4:c.1244-468T>C
ATP8B4 transcript variant X1 XM_011522046.3:c.1439-468= XM_011522046.3:c.1439-468T>C
ATP8B4 transcript variant X3 XM_011522047.3:c.1328-468= XM_011522047.3:c.1328-468T>C
ATP8B4 transcript variant X6 XM_011522048.2:c.1328-468= XM_011522048.2:c.1328-468T>C
ATP8B4 transcript variant X5 XM_011522049.3:c.1328-468= XM_011522049.3:c.1328-468T>C
ATP8B4 transcript variant X7 XM_011522052.4:c.1328-468= XM_011522052.4:c.1328-468T>C
ATP8B4 transcript variant X4 XM_011522053.2:c.1328-468= XM_011522053.2:c.1328-468T>C
ATP8B4 transcript variant X21 XM_011522056.4:c.1328-468= XM_011522056.4:c.1328-468T>C
ATP8B4 transcript variant X24 XM_011522058.4:c.1001-468= XM_011522058.4:c.1001-468T>C
ATP8B4 transcript variant X25 XM_011522059.1:c.983-468= XM_011522059.1:c.983-468T>C
ATP8B4 transcript variant X26 XM_011522060.1:c.947-468= XM_011522060.1:c.947-468T>C
ATP8B4 transcript variant X27 XM_011522061.1:c.947-468= XM_011522061.1:c.947-468T>C
ATP8B4 transcript variant X28 XM_011522062.1:c.947-468= XM_011522062.1:c.947-468T>C
ATP8B4 transcript variant X29 XM_011522063.1:c.947-468= XM_011522063.1:c.947-468T>C
ATP8B4 transcript variant X38 XM_011522069.2:c.479-468= XM_011522069.2:c.479-468T>C
ATP8B4 transcript variant X13 XM_017022587.3:c.1244-468= XM_017022587.3:c.1244-468T>C
ATP8B4 transcript variant X9 XM_017022591.2:c.1328-468= XM_017022591.2:c.1328-468T>C
ATP8B4 transcript variant X23 XM_017022594.1:c.1001-468= XM_017022594.1:c.1001-468T>C
ATP8B4 transcript variant X2 XM_024450065.2:c.1355-468= XM_024450065.2:c.1355-468T>C
ATP8B4 transcript variant X10 XM_024450066.2:c.1280-468= XM_024450066.2:c.1280-468T>C
ATP8B4 transcript variant X11 XM_024450067.2:c.1439-468= XM_024450067.2:c.1439-468T>C
ATP8B4 transcript variant X32 XM_024450068.2:c.1439-468= XM_024450068.2:c.1439-468T>C
ATP8B4 transcript variant X35 XM_024450069.1:c.692-468= XM_024450069.1:c.692-468T>C
ATP8B4 transcript variant X42 XM_024450070.2:c.1439-468= XM_024450070.2:c.1439-468T>C
ATP8B4 transcript variant X8 XM_047433082.1:c.1328-468= XM_047433082.1:c.1328-468T>C
ATP8B4 transcript variant X12 XM_047433083.1:c.1244-468= XM_047433083.1:c.1244-468T>C
ATP8B4 transcript variant X14 XM_047433084.1:c.1226-468= XM_047433084.1:c.1226-468T>C
ATP8B4 transcript variant X15 XM_047433085.1:c.1196-468= XM_047433085.1:c.1196-468T>C
ATP8B4 transcript variant X16 XM_047433086.1:c.1355-468= XM_047433086.1:c.1355-468T>C
ATP8B4 transcript variant X17 XM_047433087.1:c.1142-468= XM_047433087.1:c.1142-468T>C
ATP8B4 transcript variant X18 XM_047433088.1:c.1115-468= XM_047433088.1:c.1115-468T>C
ATP8B4 transcript variant X19 XM_047433089.1:c.1244-468= XM_047433089.1:c.1244-468T>C
ATP8B4 transcript variant X20 XM_047433090.1:c.1031-468= XM_047433090.1:c.1031-468T>C
ATP8B4 transcript variant X22 XM_047433091.1:c.1196-468= XM_047433091.1:c.1196-468T>C
ATP8B4 transcript variant X30 XM_047433092.1:c.917-468= XM_047433092.1:c.917-468T>C
ATP8B4 transcript variant X31 XM_047433093.1:c.1085-468= XM_047433093.1:c.1085-468T>C
ATP8B4 transcript variant X33 XM_047433094.1:c.1031-468= XM_047433094.1:c.1031-468T>C
ATP8B4 transcript variant X34 XM_047433096.1:c.1031-468= XM_047433096.1:c.1031-468T>C
ATP8B4 transcript variant X36 XM_047433097.1:c.611-468= XM_047433097.1:c.611-468T>C
ATP8B4 transcript variant X37 XM_047433098.1:c.611-468= XM_047433098.1:c.611-468T>C
ATP8B4 transcript variant X39 XM_047433099.1:c.1244-468= XM_047433099.1:c.1244-468T>C
ATP8B4 transcript variant X40 XM_047433100.1:c.1439-468= XM_047433100.1:c.1439-468T>C
Help

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#.

25 SubSNP, 11 Frequency submissions
No Submitter Submission ID Date (Build)
1 1000GENOMES ss338768854 May 09, 2011 (134)
2 EVA-GONL ss991770943 Aug 21, 2014 (142)
3 1000GENOMES ss1353405466 Aug 21, 2014 (142)
4 EVA_UK10K_ALSPAC ss1632965598 Apr 01, 2015 (144)
5 EVA_UK10K_TWINSUK ss1675959631 Apr 01, 2015 (144)
6 EVA_DECODE ss1695787791 Apr 01, 2015 (144)
7 HUMAN_LONGEVITY ss2206655018 Dec 20, 2016 (150)
8 GNOMAD ss2934739435 Nov 08, 2017 (151)
9 SWEGEN ss3013258157 Nov 08, 2017 (151)
10 ILLUMINA ss3021631831 Nov 08, 2017 (151)
11 ILLUMINA ss3652032421 Oct 12, 2018 (152)
12 EGCUT_WGS ss3680399697 Jul 13, 2019 (153)
13 EVA_DECODE ss3697862733 Jul 13, 2019 (153)
14 ILLUMINA ss3725498522 Jul 13, 2019 (153)
15 ACPOP ss3740910055 Jul 13, 2019 (153)
16 SGDP_PRJ ss3882886259 Apr 27, 2020 (154)
17 TOPMED ss4990881574 Apr 26, 2021 (155)
18 1000G_HIGH_COVERAGE ss5298390118 Oct 17, 2022 (156)
19 EVA ss5419144713 Oct 17, 2022 (156)
20 HUGCELL_USP ss5492124245 Oct 17, 2022 (156)
21 1000G_HIGH_COVERAGE ss5599770246 Oct 17, 2022 (156)
22 SANFORD_IMAGENETICS ss5657480529 Oct 17, 2022 (156)
23 EVA ss5828181643 Oct 17, 2022 (156)
24 EVA ss5875817697 Oct 17, 2022 (156)
25 EVA ss5948880027 Oct 17, 2022 (156)
26 1000Genomes NC_000015.9 - 50254685 Oct 12, 2018 (152)
27 1000Genomes_30x NC_000015.10 - 49962488 Oct 17, 2022 (156)
28 The Avon Longitudinal Study of Parents and Children NC_000015.9 - 50254685 Oct 12, 2018 (152)
29 Genetic variation in the Estonian population NC_000015.9 - 50254685 Oct 12, 2018 (152)
30 gnomAD - Genomes NC_000015.10 - 49962488 Apr 26, 2021 (155)
31 Genome of the Netherlands Release 5 NC_000015.9 - 50254685 Apr 27, 2020 (154)
32 Northern Sweden NC_000015.9 - 50254685 Jul 13, 2019 (153)
33 SGDP_PRJ NC_000015.9 - 50254685 Apr 27, 2020 (154)
34 TopMed NC_000015.10 - 49962488 Apr 26, 2021 (155)
35 UK 10K study - Twins NC_000015.9 - 50254685 Oct 12, 2018 (152)
36 ALFA NC_000015.10 - 49962488 Apr 26, 2021 (155)
Help

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).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss1695787791 NC_000015.8:48041976:A:G NC_000015.10:49962487:A:G (self)
66475299, 36900926, 26137945, 16479815, 14194920, 34903239, 36900926, ss338768854, ss991770943, ss1353405466, ss1632965598, ss1675959631, ss2934739435, ss3013258157, ss3021631831, ss3652032421, ss3680399697, ss3740910055, ss3882886259, ss5419144713, ss5657480529, ss5828181643, ss5948880027 NC_000015.9:50254684:A:G NC_000015.10:49962487:A:G (self)
87296181, 468647134, 206427234, 6318381068, ss2206655018, ss3697862733, ss3725498522, ss4990881574, ss5298390118, ss5492124245, ss5599770246, ss5875817697 NC_000015.10:49962487:A:G NC_000015.10:49962487:A:G (self)
Help

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

No publications for rs147936885

Help

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.

Software version is: 2.0.1.post761+d5e8e07