Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 7:107919098 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930190

Most severe consequence
Clinical significance

Synonyms

LSDB 6380

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

7:g.107919098C>T
ENST00000205402.6:c.1463C>T
ENSP00000205402.3:p.Pro488Leu
ENST00000417551.2:c.1463C>T
ENSP00000390667.1:p.Pro488Leu
ENST00000437604.3:c.1319C>T
ENSP00000387542.2:p.Pro440Leu
ENST00000415325.2:c.*1137C>T
ENST00000440410.2:c.1394C>T
ENSP00000417016.1:p.Pro465Leu

Variation displays