Original source

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

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

Chromosome 15:38349482 (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.38349482C>T
ENST00000299084.6:c.643C>T
ENSP00000299084.4:p.Gln215Ter

Variant allele G
15:g.38349482C>G
ENST00000299084.6:c.643C>G
ENSP00000299084.4:p.Gln215Glu

Variation displays