Original source

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

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

Chromosome 8:43197682 (forward strand) | View in location tab

Co-located

with COSMIC COSM1100121 (C/G), COSM1100122 (C/G) ; HGMD-PUBLIC CM071800

Most severe consequence
Clinical significance

Synonyms

LSDB 16750

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

8:g.43197682C>T
ENST00000521576.1:c.704C>T
ENSP00000429029.1:p.Ser235Phe
ENST00000519705.1:n.869C>T
ENST00000379644.6:c.1553C>T
ENSP00000368965.4:p.Ser518Phe
ENST00000523989.1:n.1866C>T

Variation displays