Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 7:30974112 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM010309

Most severe consequence
Clinical significance

Synonyms

LSDB 2344

This variation has 12 HGVS names - click the plus to show

7:g.30974112T>G
ENST00000409904.4:c.533T>G
ENSP00000387113.3:p.Phe178Cys
ENST00000489974.2:n.498T>G
ENST00000337750.6:c.175-317T>G
ENST00000409316.2:c.51-317T>G
ENST00000461390.1:n.193T>G
ENST00000396227.3:c.406-317T>G
ENST00000461424.2:n.301T>G
ENST00000611037.1:c.171T>G
ENST00000326139.3:c.725T>G
ENSP00000320180.2:p.Phe242Cys

Variation displays