This variation has been flagged

Variation has more than 3 different alleles

Original source

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

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

Chromosome 17:40822119 (forward strand) | View in location tab

Co-located

with COSMIC COSM1383031 (C/T) ; HGMD-PUBLIC CM941007, CM930453, CM920396 ; 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 21 HGVS names - click the plus to show

About this variant

This variant overlaps 15 transcripts and is associated with 6 phenotypes.

Variation displays