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 11:34966740 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM042447

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 12 HGVS names - click the plus to show

Variant allele T
11:g.34966740C>T
ENST00000448838.5:c.697C>T
ENSP00000389404.2:p.Gln233Ter
ENST00000430469.4:c.343-17830C>T
ENST00000227868.6:c.742C>T
ENSP00000227868.4:p.Gln248Ter

Variant allele G
11:g.34966740C>G
ENST00000448838.5:c.697C>G
ENSP00000389404.2:p.Gln233Glu
ENST00000430469.4:c.343-17830C>G
ENST00000227868.6:c.742C>G
ENSP00000227868.4:p.Gln248Glu

Variation displays