Original source

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

G/A | Ancestral: G | Ambiguity code: R

Chromosome 14:61115580 (forward strand) | View in location tab


with COSMIC COSM1300718 (G/A), COSM164343 (G/T), COSM698206 (G/C) ; HGMD-PUBLIC CM041438

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

Variation displays