Original source

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

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

Chromosome 4:1002387 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM970761

Most severe consequence
Clinical significance

Synonyms

LSDB 6459

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

4:g.1002387C>T
ENST00000514224.1:c.695C>T
ENSP00000425081.1:p.Thr232Met
ENST00000514698.3:n.1198C>T
ENST00000247933.6:c.1091C>T
ENSP00000247933.4:p.Thr364Met

Variation displays