Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 4:54733155 (forward strand) | View in location tab

Co-located

with COSMIC COSM1314 (A/T), COSM24675 (A/C), COSM12711 (A/G) ; HGMD-PUBLIC CM952169 ; PhenCode KinMutBase_KIT_DNA:g.76140A>T (A/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

Variation displays