Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 18:23535683 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990947

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

18:g.23535683T>C
ENST00000269228.7:c.3263A>G
ENSP00000269228.4:p.Tyr1088Cys
ENST00000591051.1:c.2341A>G
ENSP00000467636.1:p.Tyr781Cys
ENST00000586150.3:c.18A>G
ENSP00000468321.1:p.Tyr7Cys
ENST00000588867.1:n.18A>G

Variation displays