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 7:22978444 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM063977

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_032581.3:c.158T>C, NM_032581.2:c.158T>C, 16765

This variation has 10 HGVS names - click the plus to show

7:g.22978444A>G
ENST00000440481.2:c.313T>C
ENSP00000397168.1:p.Leu105Pro
ENST00000409763.1:c.158T>C
ENSP00000386624.1:p.Leu53Pro
ENST00000432176.3:c.158T>C
ENSP00000403396.2:p.Leu53Pro
ENST00000477349.2:n.248T>C
ENST00000409923.2:c.158T>C
ENSP00000386246.1:p.Leu53Pro

Variation displays