Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)

Chromosome 10:74074808 (forward strand) | View in location tab


with COSMIC COSM3440558 (C/T)

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB NC_000010.9:g.75504572C>T

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 6 transcripts, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays