Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 1:17033078 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012800

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_241_SDHB_185470_0001, 5495, SDHB_268C_T_061511

This variation has 13 HGVS names - click the plus to show

1:g.17033078G>A
ENST00000475506.1:n.185C>T
ENST00000491274.3:c.226C>T
ENSP00000480482.1:p.Arg76Ter
ENST00000485515.3:n.256C>T
ENST00000375499.5:c.268C>T
ENSP00000364649.3:p.Arg90Ter
ENST00000463045.2:c.97C>T
ENSP00000481376.1:p.Arg33Ter
ENST00000466613.2:n.280C>T
LRG_316:g.26093C>T
LRG_316t1:c.268C>T
LRG_316p1:p.Arg90Ter

Variation displays