Original source

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

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

Chromosome 1:17024025 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012801

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB SDHB_590C_G_110910, 5496, 2009_August_001_242_SDHB_185470_0002

This variation has 9 HGVS names - click the plus to show

1:g.17024025G>C
ENST00000491274.3:c.548C>G
ENSP00000480482.1:p.Pro183Arg
ENST00000485515.3:n.524C>G
ENST00000375499.5:c.590C>G
ENSP00000364649.3:p.Pro197Arg
LRG_316:g.35146C>G
LRG_316t1.1:c.590C>G
LRG_316p1.1:p.Pro197Arg

Variation displays