This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
A/C/G/T | Ancestral: A | Ambiguity code: N
Location

Chromosome 19:41848120 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041083, CM041084

Most severe consequence
Evidence status

Clinical significance

This variation has 9 synonyms - click the plus to show

This variation has 15 HGVS names - click the plus to show

Variant allele T
19:g.41848120A>T
ENST00000597453.1:n.198T>A
ENST00000221930.5:c.667T>A
ENSP00000221930.4:p.Cys223Ser
ENST00000600196.1:n.127T>A

Variant allele C
19:g.41848120A>C
ENST00000597453.1:n.198T>G
ENST00000221930.5:c.667T>G
ENSP00000221930.4:p.Cys223Gly
ENST00000600196.1:n.127T>G

Variant allele G
19:g.41848120A>G
ENST00000597453.1:n.198T>C
ENST00000221930.5:c.667T>C
ENSP00000221930.4:p.Cys223Arg
ENST00000600196.1:n.127T>C

Variation displays