This variation has been flagged

Variation has more than 3 different alleles

Original source

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

C/A/G/T | Ancestral: C | Ambiguity code: N

Chromosome 17:38978371 (forward strand) | View in location tab


with COSMIC COSM1383031 (C/T) ; HGMD-PUBLIC CM941007, CM920396, CM930453 ; PhenCode HIFD_KRT10:c.467G>A (C/T), HIFD_KRT10:c.467G>C (C/G), HIFD_KRT10:c.467G>T (C/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 18 HGVS names - click the plus to show

Variation displays