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

Chromosome 19:55154146 (forward strand) | View in location tab

Co-located

with COSMIC COSM475295 (G/A) ; HGMD-PUBLIC CM971498, CM030285 ; PhenCode FHC0405 (G/A), FHC0407 (G/C)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 7 synonyms - click the plus to show

This variant has 30 HGVS names - click the plus to show

About this variant

This variant overlaps 87 transcripts and is associated with 6 phenotypes.

Variant displays