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 6:43610596 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM991065

Most severe consequence
Clinical significance

Synonyms

LSDB 12334

This variation has 9 HGVS names - click the plus to show

6:g.43610596C>T
ENST00000372226.1:c.1117C>T
ENSP00000361300.1:p.Gln373Ter
ENST00000496137.3:c.*132-5214G>A
ENST00000372236.6:c.1117C>T
ENSP00000361310.4:p.Gln373Ter
LRG_470:g.39456C>T
LRG_470t1.1:c.1117C>T
LRG_470p1.1:p.Gln373Ter

Variation displays