Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 17:44908075 (forward strand) | View in location tab

Co-located

with COSMIC COSM980059 (G/A) ; HGMD-PUBLIC CM010052 ; PhenCode HIFD_GFAP:c.1246C>T (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2165, GFAP:c.1246C>T

This variation has 19 HGVS names - click the plus to show

Variant allele A
17:g.44908075G>A
ENST00000592706.2:n.118C>T
ENST00000592065.1:n.40C>T
ENST00000591880.1:c.112C>T
ENSP00000467530.1:p.Arg38Trp
ENST00000253408.6:c.1246C>T
ENSP00000253408.4:p.Arg416Trp
ENST00000589701.1:n.148C>T
ENST00000585543.2:n.399C>T
ENST00000588735.1:c.124C>T
ENSP00000466598.1:p.Arg42Trp

Variant allele T
17:g.44908075G>T
ENST00000592706.2:n.118C>A
ENST00000592065.1:n.40C>A
ENST00000591880.1:c.112C>A
ENST00000253408.6:c.1246C>A
ENST00000589701.1:n.148C>A
ENST00000585543.2:n.399C>A
ENST00000588735.1:c.124C>A

Variation displays