Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 4:996121 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM000404

Most severe consequence
Clinical significance

Synonyms

LSDB 6461

This variation has 8 HGVS names - click the plus to show

4:g.996121T>G
ENST00000514224.1:c.641T>G
ENSP00000425081.1:p.Leu214Arg
ENST00000514698.1:n.1144T>G
ENST00000453894.1:c.1103T>G
ENSP00000396458.1:p.Leu368Arg
ENST00000247933.4:c.1037T>G
ENSP00000247933.4:p.Leu346Arg

Variation displays