Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 4:997206 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981063, CM920373

Most severe consequence
Clinical significance

Synonyms

LSDB 6444

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

4:g.997206C>G
ENST00000514224.1:c.1202C>G
ENSP00000425081.1:p.Pro401Arg
ENST00000514698.1:n.1705C>G
ENST00000453894.1:c.1664C>G
ENSP00000396458.1:p.Pro555Arg
ENST00000247933.4:c.1598C>G
ENSP00000247933.4:p.Pro533Arg

Variation displays