Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 9:91757380 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM052360

Most severe consequence
Clinical significance

Synonyms

LSDB 10993

This variation has 7 HGVS names - click the plus to show

9:g.91757380G>A
ENST00000550066.3:n.823C>T
ENST00000495386.3:n.618C>T
ENST00000375715.3:c.-66C>T
ENST00000375708.3:c.355C>T
ENSP00000364860.3:p.Arg119Ter
ENST00000548585.2:n.172+49C>T

Variation displays