Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 11:111957634 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM092619, CM013281

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11382, 2010_April_001_300_SDHD_602690_0015, NM_003002.1:c.3G>C

This variation has 19 HGVS names - click the plus to show

11:g.111957634G>C
ENST00000528182.1:c.3G>C
ENSP00000435475.1:p.Met1?
ENST00000525987.1:n.8G>C
ENST00000526592.1:c.3G>C
ENSP00000432005.1:p.Met1?
HG388_HG400_PATCH:g.111957633G>C
ENST00000532699.1:c.3G>C
ENSP00000456434.1:p.Met1?
ENST00000375549.3:c.3G>C
ENSP00000364699.3:p.Met1?
ENST00000528021.1:c.3G>C
ENSP00000432465.1:p.Met1?
ENST00000525291.1:c.3G>C
ENSP00000436669.1:p.Met1?
ENST00000531744.1:c.3G>C
ENSP00000456957.1:p.Met1?
ENST00000528048.1:c.3G>C
ENSP00000436217.1:p.Met1?

Variation displays