Original source

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

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

Chromosome 11:111957645 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020972

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_306_SDHD_602690_0026, 11393

This variation has 21 HGVS names - click the plus to show

11:g.111957645G>A
ENST00000528182.1:c.14G>A
ENSP00000435475.1:p.Trp5Ter
ENST00000525987.1:n.19G>A
ENST00000526592.1:c.14G>A
ENSP00000432005.1:p.Trp5Ter
HG388_HG400_PATCH:g.111957644G>A
ENST00000532699.1:c.14G>A
ENSP00000456434.1:p.Trp5Ter
ENST00000375549.3:c.14G>A
ENSP00000364699.3:p.Trp5Ter
ENST00000528021.1:c.14G>A
ENSP00000432465.1:p.Trp5Ter
ENST00000525291.1:c.14G>A
ENSP00000436669.1:p.Trp5Ter
ENST00000531744.1:c.14G>A
ENSP00000456957.1:p.Trp5Ter
ENST00000530923.1:c.4G>A
ENSP00000432946.1:p.Trp2Ter
ENST00000528048.1:c.14G>A
ENSP00000436217.1:p.Trp5Ter

Variation displays