This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
T/A/C/G | Ancestral: T | Ambiguity code: N
Location

Chromosome 5:150054082 (forward strand) | View in location tab

Co-located

with COSMIC COSM948 (T/A), COSM947 (T/C) ; HGMD-PUBLIC CM900079

Most severe consequence

This variation has 5 synonyms - click the plus to show

This variation has 15 HGVS names - click the plus to show

About this variant

This variant overlaps 24 transcripts and has 1 individual genotype.

Variation displays