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 3:57198214 (forward strand) | View in location tab

Co-located

with COSMIC COSM1424823 (T/A) ; HGMD-PUBLIC CM010056

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 10619, 2010_April_001_119_HESX1_601802_0003

This variation has 5 HGVS names - click the plus to show

3:g.57198214T>C
ENST00000473921.2:c.439A>G
ENSP00000418918.1:p.Thr147Ala
ENST00000295934.5:c.541A>G
ENSP00000295934.3:p.Thr181Ala

Variation displays