Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 11:112094831 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012466, CD062227

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11374, 2010_April_001_296_SDHD_602690_0007

This variation has 16 HGVS names - click the plus to show

11:g.112094831A>G
ENST00000532699.1:c.314+5820A>G
ENST00000528182.3:c.334A>G
ENSP00000435475.1:p.Met112Val
ENST00000525987.3:n.319+5820A>G
ENST00000534010.1:c.145+5820A>G
ENST00000526592.3:c.*39A>G
ENST00000375549.5:c.341A>G
ENSP00000364699.3:p.Tyr114Cys
ENST00000525291.3:c.224A>G
ENSP00000436669.1:p.Tyr75Cys
ENST00000528021.3:c.314+5820A>G
ENST00000531744.3:c.314+5820A>G
ENST00000530923.3:c.*80A>G
ENST00000528048.3:c.196A>G
ENSP00000436217.1:p.Met66Val

Variation displays