Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 9:35078335 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM982051 ; PhenCode FANCG:c.313G>T (C/A)

Most severe consequence
Clinical significance

Synonyms

LSDB 11551

This variation has 10 HGVS names - click the plus to show

9:g.35078335C>A
ENST00000448890.1:c.313G>T
ENSP00000409607.1:p.Glu105Ter
ENST00000425676.1:c.307+267G>T
ENST00000461149.1:n.48G>T
ENST00000378643.3:c.313G>T
ENSP00000367910.3:p.Glu105Ter
LRG_499:g.6679G>T
LRG_499t1.1:c.313G>T
LRG_499p1.1:p.Glu105Ter

Variation displays