Original source

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

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

Chromosome 7:143342001 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM950274

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 3 HGVS names - click the plus to show

7:g.143342001A>G
ENST00000343257.4:c.1655A>G
ENSP00000339867.2:p.Gln552Arg

Variation displays