Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 15:38641683 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM074581

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 16208

This variation has 6 HGVS names - click the plus to show

Variant allele T
15:g.38641683C>T
ENST00000299084.4:c.643C>T
ENSP00000299084.4:p.Gln215Ter

Variant allele G
15:g.38641683C>G
ENST00000299084.4:c.643C>G
ENSP00000299084.4:p.Gln215Glu

Variation displays