Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 12:90964302 (forward strand) | View in location tab

Co-located

with COSMIC COSM108033 (C/T) ; ESP TMP_ESP_12_91358079_91358079 (C/T)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000012.10:g.89882210C>T

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript, is associated with 1 phenotype and is mentioned in 1 citation.

Somatic mutation displays