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 11:112086908 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM044712

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_303_SDHD_602690_0021, 11388

This variation has 20 HGVS names - click the plus to show

11:g.112086908A>G
ENST00000528182.3:c.1A>G
ENSP00000435475.1:p.Met1?
ENST00000525987.3:n.6A>G
ENST00000526592.3:c.1A>G
ENSP00000432005.1:p.Met1?
ENST00000614349.2:c.1A>G
ENSP00000480666.1:p.Met1?
ENST00000532699.1:c.1A>G
ENSP00000456434.1:p.Met1?
ENST00000375549.5:c.1A>G
ENSP00000364699.3:p.Met1?
ENST00000528021.3:c.1A>G
ENSP00000432465.1:p.Met1?
ENST00000525291.3:c.1A>G
ENSP00000436669.1:p.Met1?
ENST00000531744.3:c.1A>G
ENSP00000456957.1:p.Met1?
ENST00000528048.3:c.1A>G
ENSP00000436217.1:p.Met1?

Variation displays