Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs1490221828

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr17:75588299 (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
G>A / G>C
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.000008 (2/264690, TOPMED)
A=0.00000 (0/10680, ALFA)
C=0.00000 (0/10680, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
MYO15B : Missense 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 10680 G=1.00000 A=0.00000, C=0.00000 1.0 0.0 0.0 N/A
European Sub 6962 G=1.0000 A=0.0000, C=0.0000 1.0 0.0 0.0 N/A
African Sub 2294 G=1.0000 A=0.0000, C=0.0000 1.0 0.0 0.0 N/A
African Others Sub 84 G=1.00 A=0.00, C=0.00 1.0 0.0 0.0 N/A
African American Sub 2210 G=1.0000 A=0.0000, C=0.0000 1.0 0.0 0.0 N/A
Asian Sub 108 G=1.000 A=0.000, C=0.000 1.0 0.0 0.0 N/A
East Asian Sub 84 G=1.00 A=0.00, C=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 24 G=1.00 A=0.00, C=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 146 G=1.000 A=0.000, C=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 610 G=1.000 A=0.000, C=0.000 1.0 0.0 0.0 N/A
South Asian Sub 94 G=1.00 A=0.00, C=0.00 1.0 0.0 0.0 N/A
Other Sub 466 G=1.000 A=0.000, C=0.000 1.0 0.0 0.0 N/A


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 G=0.999992 A=0.000008
Allele Frequency Aggregator Total Global 10680 G=1.00000 A=0.00000, C=0.00000
Allele Frequency Aggregator European Sub 6962 G=1.0000 A=0.0000, C=0.0000
Allele Frequency Aggregator African Sub 2294 G=1.0000 A=0.0000, C=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 G=1.000 A=0.000, C=0.000
Allele Frequency Aggregator Other Sub 466 G=1.000 A=0.000, C=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 G=1.000 A=0.000, C=0.000
Allele Frequency Aggregator Asian Sub 108 G=1.000 A=0.000, C=0.000
Allele Frequency Aggregator South Asian Sub 94 G=1.00 A=0.00, C=0.00
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 17 NC_000017.11:g.75588299G>A
GRCh38.p14 chr 17 NC_000017.11:g.75588299G>C
GRCh37.p13 chr 17 NC_000017.10:g.73584380G>A
GRCh37.p13 chr 17 NC_000017.10:g.73584380G>C
Gene: MYO15B, myosin XVB (plus strand)
Molecule type Change Amino acid[Codon] SO Term
MYO15B transcript variant 2 NM_001309242.1:c.242G>A G [GGG] > E [GAG] Coding Sequence Variant
myosin XVB isoform 2 NP_001296171.1:p.Gly81Glu G (Gly) > E (Glu) Missense Variant
MYO15B transcript variant 2 NM_001309242.1:c.242G>C G [GGG] > A [GCG] Coding Sequence Variant
myosin XVB isoform 2 NP_001296171.1:p.Gly81Ala G (Gly) > A (Ala) Missense Variant
MYO15B transcript variant 1 NM_001395058.1:c.242G>A G [GGG] > E [GAG] Coding Sequence Variant
myosin XVB isoform 1 NP_001381987.1:p.Gly81Glu G (Gly) > E (Glu) Missense Variant
MYO15B transcript variant 1 NM_001395058.1:c.242G>C G [GGG] > A [GCG] Coding Sequence Variant
myosin XVB isoform 1 NP_001381987.1:p.Gly81Ala G (Gly) > A (Ala) Missense Variant
MYO15B transcript variant X11 XM_017025129.3:c. N/A Genic Upstream Transcript Variant
MYO15B transcript variant X12 XM_017025130.3:c. N/A Genic Upstream Transcript Variant
MYO15B transcript variant X13 XM_017025131.3:c. N/A Genic Upstream Transcript Variant
MYO15B transcript variant X21 XM_017025135.3:c. N/A Genic Upstream Transcript Variant
MYO15B transcript variant X20 XM_017025136.3:c. N/A Genic Upstream Transcript Variant
MYO15B transcript variant X22 XM_017025137.3:c. N/A Genic Upstream Transcript Variant
MYO15B transcript variant X24 XM_017025138.3:c. N/A Genic Upstream Transcript Variant
MYO15B transcript variant X26 XM_017025140.3:c. N/A Genic Upstream Transcript Variant
MYO15B transcript variant X28 XM_017025143.3:c. N/A Genic Upstream Transcript Variant
MYO15B transcript variant X29 XM_024450952.2:c. N/A Genic Upstream Transcript Variant
MYO15B transcript variant X14 XM_047436790.1:c. N/A Genic Upstream Transcript Variant
MYO15B transcript variant X15 XM_047436791.1:c. N/A Genic Upstream Transcript Variant
MYO15B transcript variant X16 XM_047436792.1:c. N/A Genic Upstream Transcript Variant
MYO15B transcript variant X17 XM_047436793.1:c. N/A Genic Upstream Transcript Variant
MYO15B transcript variant X18 XM_047436794.1:c. N/A Genic Upstream Transcript Variant
MYO15B transcript variant X25 XM_047436797.1:c. N/A Genic Upstream Transcript Variant
MYO15B transcript variant X1 XM_017025120.3:c.242G>A G [GGG] > E [GAG] Coding Sequence Variant
myosin XVB isoform X1 XP_016880609.1:p.Gly81Glu G (Gly) > E (Glu) Missense Variant
MYO15B transcript variant X1 XM_017025120.3:c.242G>C G [GGG] > A [GCG] Coding Sequence Variant
myosin XVB isoform X1 XP_016880609.1:p.Gly81Ala G (Gly) > A (Ala) Missense Variant
MYO15B transcript variant X2 XM_017025121.3:c.242G>A G [GGG] > E [GAG] Coding Sequence Variant
myosin XVB isoform X2 XP_016880610.1:p.Gly81Glu G (Gly) > E (Glu) Missense Variant
MYO15B transcript variant X2 XM_017025121.3:c.242G>C G [GGG] > A [GCG] Coding Sequence Variant
myosin XVB isoform X2 XP_016880610.1:p.Gly81Ala G (Gly) > A (Ala) Missense Variant
MYO15B transcript variant X3 XM_017025122.3:c.242G>A G [GGG] > E [GAG] Coding Sequence Variant
myosin XVB isoform X3 XP_016880611.1:p.Gly81Glu G (Gly) > E (Glu) Missense Variant
MYO15B transcript variant X3 XM_017025122.3:c.242G>C G [GGG] > A [GCG] Coding Sequence Variant
myosin XVB isoform X3 XP_016880611.1:p.Gly81Ala G (Gly) > A (Ala) Missense Variant
MYO15B transcript variant X4 XM_017025123.3:c.242G>A G [GGG] > E [GAG] Coding Sequence Variant
myosin XVB isoform X4 XP_016880612.1:p.Gly81Glu G (Gly) > E (Glu) Missense Variant
MYO15B transcript variant X4 XM_017025123.3:c.242G>C G [GGG] > A [GCG] Coding Sequence Variant
myosin XVB isoform X4 XP_016880612.1:p.Gly81Ala G (Gly) > A (Ala) Missense Variant
MYO15B transcript variant X5 XM_017025124.3:c.242G>A G [GGG] > E [GAG] Coding Sequence Variant
myosin XVB isoform X5 XP_016880613.1:p.Gly81Glu G (Gly) > E (Glu) Missense Variant
MYO15B transcript variant X5 XM_017025124.3:c.242G>C G [GGG] > A [GCG] Coding Sequence Variant
myosin XVB isoform X5 XP_016880613.1:p.Gly81Ala G (Gly) > A (Ala) Missense Variant
MYO15B transcript variant X6 XM_017025125.3:c.242G>A G [GGG] > E [GAG] Coding Sequence Variant
myosin XVB isoform X6 XP_016880614.1:p.Gly81Glu G (Gly) > E (Glu) Missense Variant
MYO15B transcript variant X6 XM_017025125.3:c.242G>C G [GGG] > A [GCG] Coding Sequence Variant
myosin XVB isoform X6 XP_016880614.1:p.Gly81Ala G (Gly) > A (Ala) Missense Variant
MYO15B transcript variant X7 XM_047436788.1:c.242G>A G [GGG] > E [GAG] Coding Sequence Variant
myosin XVB isoform X7 XP_047292744.1:p.Gly81Glu G (Gly) > E (Glu) Missense Variant
MYO15B transcript variant X7 XM_047436788.1:c.242G>C G [GGG] > A [GCG] Coding Sequence Variant
myosin XVB isoform X7 XP_047292744.1:p.Gly81Ala G (Gly) > A (Ala) Missense Variant
MYO15B transcript variant X8 XM_017025127.3:c.242G>A G [GGG] > E [GAG] Coding Sequence Variant
myosin XVB isoform X8 XP_016880616.1:p.Gly81Glu G (Gly) > E (Glu) Missense Variant
MYO15B transcript variant X8 XM_017025127.3:c.242G>C G [GGG] > A [GCG] Coding Sequence Variant
myosin XVB isoform X8 XP_016880616.1:p.Gly81Ala G (Gly) > A (Ala) Missense Variant
MYO15B transcript variant X9 XM_017025128.3:c.151G>A G [GGG] > R [AGG] Coding Sequence Variant
myosin XVB isoform X9 XP_016880617.1:p.Gly51Arg G (Gly) > R (Arg) Missense Variant
MYO15B transcript variant X9 XM_017025128.3:c.151G>C G [GGG] > R [CGG] Coding Sequence Variant
myosin XVB isoform X9 XP_016880617.1:p.Gly51Arg G (Gly) > R (Arg) Missense Variant
MYO15B transcript variant X10 XM_047436789.1:c.242G>A G [GGG] > E [GAG] Coding Sequence Variant
myosin XVB isoform X10 XP_047292745.1:p.Gly81Glu G (Gly) > E (Glu) Missense Variant
MYO15B transcript variant X10 XM_047436789.1:c.242G>C G [GGG] > A [GCG] Coding Sequence Variant
myosin XVB isoform X10 XP_047292745.1:p.Gly81Ala G (Gly) > A (Ala) Missense Variant
MYO15B transcript variant X19 XM_047436795.1:c.242G>A G [GGG] > E [GAG] Coding Sequence Variant
myosin XVB isoform X19 XP_047292751.1:p.Gly81Glu G (Gly) > E (Glu) Missense Variant
MYO15B transcript variant X19 XM_047436795.1:c.242G>C G [GGG] > A [GCG] Coding Sequence Variant
myosin XVB isoform X19 XP_047292751.1:p.Gly81Ala G (Gly) > A (Ala) Missense Variant
MYO15B transcript variant X23 XM_047436796.1:c.242G>A G [GGG] > E [GAG] Coding Sequence Variant
myosin XVB isoform X22 XP_047292752.1:p.Gly81Glu G (Gly) > E (Glu) Missense Variant
MYO15B transcript variant X23 XM_047436796.1:c.242G>C G [GGG] > A [GCG] Coding Sequence Variant
myosin XVB isoform X22 XP_047292752.1:p.Gly81Ala G (Gly) > A (Ala) Missense Variant
MYO15B transcript variant X27 XM_047436798.1:c.242G>A G [GGG] > E [GAG] Coding Sequence Variant
myosin XVB isoform X26 XP_047292754.1:p.Gly81Glu G (Gly) > E (Glu) Missense Variant
MYO15B transcript variant X27 XM_047436798.1:c.242G>C G [GGG] > A [GCG] Coding Sequence Variant
myosin XVB isoform X26 XP_047292754.1:p.Gly81Ala G (Gly) > A (Ala) Missense 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 G= A C
GRCh38.p14 chr 17 NC_000017.11:g.75588299= NC_000017.11:g.75588299G>A NC_000017.11:g.75588299G>C
GRCh37.p13 chr 17 NC_000017.10:g.73584380= NC_000017.10:g.73584380G>A NC_000017.10:g.73584380G>C
MYO15B transcript variant X1 XM_017025120.3:c.242= XM_017025120.3:c.242G>A XM_017025120.3:c.242G>C
MYO15B transcript variant X1 XM_017025120.2:c.242= XM_017025120.2:c.242G>A XM_017025120.2:c.242G>C
MYO15B transcript variant X1 XM_017025120.1:c.242= XM_017025120.1:c.242G>A XM_017025120.1:c.242G>C
MYO15B transcript variant X2 XM_017025121.3:c.242= XM_017025121.3:c.242G>A XM_017025121.3:c.242G>C
MYO15B transcript variant X2 XM_017025121.2:c.242= XM_017025121.2:c.242G>A XM_017025121.2:c.242G>C
MYO15B transcript variant X2 XM_017025121.1:c.242= XM_017025121.1:c.242G>A XM_017025121.1:c.242G>C
MYO15B transcript variant X3 XM_017025122.3:c.242= XM_017025122.3:c.242G>A XM_017025122.3:c.242G>C
MYO15B transcript variant X3 XM_017025122.2:c.242= XM_017025122.2:c.242G>A XM_017025122.2:c.242G>C
MYO15B transcript variant X3 XM_017025122.1:c.242= XM_017025122.1:c.242G>A XM_017025122.1:c.242G>C
MYO15B transcript variant X4 XM_017025123.3:c.242= XM_017025123.3:c.242G>A XM_017025123.3:c.242G>C
MYO15B transcript variant X4 XM_017025123.2:c.242= XM_017025123.2:c.242G>A XM_017025123.2:c.242G>C
MYO15B transcript variant X4 XM_017025123.1:c.242= XM_017025123.1:c.242G>A XM_017025123.1:c.242G>C
MYO15B transcript variant X5 XM_017025124.3:c.242= XM_017025124.3:c.242G>A XM_017025124.3:c.242G>C
MYO15B transcript variant X5 XM_017025124.2:c.242= XM_017025124.2:c.242G>A XM_017025124.2:c.242G>C
MYO15B transcript variant X5 XM_017025124.1:c.242= XM_017025124.1:c.242G>A XM_017025124.1:c.242G>C
MYO15B transcript variant X6 XM_017025125.3:c.242= XM_017025125.3:c.242G>A XM_017025125.3:c.242G>C
MYO15B transcript variant X6 XM_017025125.2:c.242= XM_017025125.2:c.242G>A XM_017025125.2:c.242G>C
MYO15B transcript variant X6 XM_017025125.1:c.242= XM_017025125.1:c.242G>A XM_017025125.1:c.242G>C
MYO15B transcript variant X8 XM_017025127.3:c.242= XM_017025127.3:c.242G>A XM_017025127.3:c.242G>C
MYO15B transcript variant X9 XM_017025127.2:c.242= XM_017025127.2:c.242G>A XM_017025127.2:c.242G>C
MYO15B transcript variant X9 XM_017025127.1:c.242= XM_017025127.1:c.242G>A XM_017025127.1:c.242G>C
MYO15B transcript variant X9 XM_017025128.3:c.151= XM_017025128.3:c.151G>A XM_017025128.3:c.151G>C
MYO15B transcript variant X10 XM_017025128.2:c.151= XM_017025128.2:c.151G>A XM_017025128.2:c.151G>C
MYO15B transcript variant X10 XM_017025128.1:c.151= XM_017025128.1:c.151G>A XM_017025128.1:c.151G>C
MYO15B transcript variant 2 NM_001309242.2:c.242= NM_001309242.2:c.242G>A NM_001309242.2:c.242G>C
MYO15B transcript variant 2 NM_001309242.1:c.242= NM_001309242.1:c.242G>A NM_001309242.1:c.242G>C
MYO15B transcript NR_003587.2:n.242= NR_003587.2:n.242G>A NR_003587.2:n.242G>C
MYO15B transcript variant 1 NM_001395058.1:c.242= NM_001395058.1:c.242G>A NM_001395058.1:c.242G>C
MYO15B transcript variant X7 XM_047436788.1:c.242= XM_047436788.1:c.242G>A XM_047436788.1:c.242G>C
MYO15B transcript variant X10 XM_047436789.1:c.242= XM_047436789.1:c.242G>A XM_047436789.1:c.242G>C
MYO15B transcript variant X19 XM_047436795.1:c.242= XM_047436795.1:c.242G>A XM_047436795.1:c.242G>C
MYO15B transcript variant X23 XM_047436796.1:c.242= XM_047436796.1:c.242G>A XM_047436796.1:c.242G>C
MYO15B transcript variant X27 XM_047436798.1:c.242= XM_047436798.1:c.242G>A XM_047436798.1:c.242G>C
myosin XVB isoform X1 XP_016880609.1:p.Gly81= XP_016880609.1:p.Gly81Glu XP_016880609.1:p.Gly81Ala
myosin XVB isoform X2 XP_016880610.1:p.Gly81= XP_016880610.1:p.Gly81Glu XP_016880610.1:p.Gly81Ala
myosin XVB isoform X3 XP_016880611.1:p.Gly81= XP_016880611.1:p.Gly81Glu XP_016880611.1:p.Gly81Ala
myosin XVB isoform X4 XP_016880612.1:p.Gly81= XP_016880612.1:p.Gly81Glu XP_016880612.1:p.Gly81Ala
myosin XVB isoform X5 XP_016880613.1:p.Gly81= XP_016880613.1:p.Gly81Glu XP_016880613.1:p.Gly81Ala
myosin XVB isoform X6 XP_016880614.1:p.Gly81= XP_016880614.1:p.Gly81Glu XP_016880614.1:p.Gly81Ala
myosin XVB isoform X8 XP_016880616.1:p.Gly81= XP_016880616.1:p.Gly81Glu XP_016880616.1:p.Gly81Ala
myosin XVB isoform X9 XP_016880617.1:p.Gly51= XP_016880617.1:p.Gly51Arg XP_016880617.1:p.Gly51Arg
myosin XVB isoform 2 NP_001296171.1:p.Gly81= NP_001296171.1:p.Gly81Glu NP_001296171.1:p.Gly81Ala
myosin XVB isoform 1 NP_001381987.1:p.Gly81= NP_001381987.1:p.Gly81Glu NP_001381987.1:p.Gly81Ala
myosin XVB isoform X7 XP_047292744.1:p.Gly81= XP_047292744.1:p.Gly81Glu XP_047292744.1:p.Gly81Ala
myosin XVB isoform X10 XP_047292745.1:p.Gly81= XP_047292745.1:p.Gly81Glu XP_047292745.1:p.Gly81Ala
myosin XVB isoform X19 XP_047292751.1:p.Gly81= XP_047292751.1:p.Gly81Glu XP_047292751.1:p.Gly81Ala
myosin XVB isoform X22 XP_047292752.1:p.Gly81= XP_047292752.1:p.Gly81Glu XP_047292752.1:p.Gly81Ala
myosin XVB isoform X26 XP_047292754.1:p.Gly81= XP_047292754.1:p.Gly81Glu XP_047292754.1:p.Gly81Ala
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#.

2 SubSNP, 4 Frequency submissions
No Submitter Submission ID Date (Build)
1 GNOMAD ss2952506875 Nov 08, 2017 (151)
2 TOPMED ss5043958566 Apr 27, 2021 (155)
3 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 513977718 (NC_000017.11:75588298:G:A 1/140318)
Row 513977719 (NC_000017.11:75588298:G:C 1/140318)

- Apr 27, 2021 (155)
4 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 513977718 (NC_000017.11:75588298:G:A 1/140318)
Row 513977719 (NC_000017.11:75588298:G:C 1/140318)

- Apr 27, 2021 (155)
5 TopMed NC_000017.11 - 75588299 Apr 27, 2021 (155)
6 ALFA NC_000017.11 - 75588299 Apr 27, 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
259504228, 7990547916, ss5043958566 NC_000017.11:75588298:G:A NC_000017.11:75588298:G:A (self)
ss2952506875 NC_000017.10:73584379:G:C NC_000017.11:75588298:G:C (self)
7990547916 NC_000017.11:75588298:G:C NC_000017.11:75588298:G:C (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 rs1490221828

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.post820+afb47a3d