Original source

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

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

Chromosome 7:143330788 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM950265

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

7:g.143330788C>G
ENST00000343257.3:c.870C>G
ENSP00000339867.2:p.Ile290Met
ENST00000455478.2:c.*155C>G
ENST00000432192.2:c.*155C>G
ENST00000495612.1:n.171C>G

Variation displays