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 8:99854202 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041281

Most severe consequence
Clinical significance

Synonyms

LSDB 15258

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

8:g.99854202C>T
ENST00000358544.3:c.10888C>T
ENSP00000351346.2:p.Gln3630Ter
ENST00000357162.3:c.10813C>T
ENSP00000349685.2:p.Gln3605Ter

Variation displays