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 10:73491908 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM010180

Most severe consequence
Clinical significance

Synonyms

LSDB 13249

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

10:g.73491908C>T
ENST00000398786.2:c.-6+5577G>A
ENST00000224721.6:c.3895C>T
ENSP00000224721.6:p.Gln1299Ter
ENST00000398792.3:n.572C>T

Variation displays