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 10:93793207 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM070982

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 12771, 2010_April_001_049_LGI1_604619_0009

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

10:g.93793207T>C
ENST00000371413.3:c.695T>C
ENSP00000360467.3:p.Leu232Pro
ENST00000371418.6:c.695T>C
ENSP00000360472.4:p.Leu232Pro

Variation displays