Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 8:100866430 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041281

Most severe consequence
Clinical significance

Synonyms

LSDB 15258

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

8:g.100866430C>T
ENST00000358544.2:c.10888C>T
ENSP00000351346.2:p.Gln3630Ter
ENST00000395996.1:c.*6671C>T
ENST00000357162.2:c.10813C>T
ENSP00000349685.2:p.Gln3605Ter

Variation displays