Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.01 (A)
Location

Chromosome 8:16155085 (forward strand) | View in location tab

Co-located

with COSMIC COSM3942587 (G/A), COSM3942588 (G/A) ; HGMD-PUBLIC CM023579

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

8:g.16155085G>A
ENST00000350896.3:c.877C>T
ENSP00000262100.3:p.Arg293Ter
ENST00000519060.5:c.*236C>T
ENST00000355282.5:c.877C>T
ENSP00000347430.2:p.Arg293Ter
ENST00000445506.5:c.931C>T
ENSP00000405453.2:p.Arg311Ter
ENST00000262101.8:c.877C>T
ENSP00000262101.5:p.Arg293Ter
ENST00000522672.4:c.247C>T
ENSP00000430536.1:p.Arg83Ter
ENST00000381998.7:c.877C>T
ENSP00000371428.4:p.Arg293Ter

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts, has 2506 individual genotypes, is associated with 3 phenotypes and is mentioned in 1 citation.

Variation displays