Original source

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

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

Chromosome 4:1003102 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM950685

Most severe consequence
Clinical significance

Synonyms

LSDB 6453

This variation has 7 HGVS names - click the plus to show

4:g.1003102T>C
ENST00000514224.1:c.1073T>C
ENSP00000425081.1:p.Leu358Pro
ENST00000514698.3:n.1576T>C
ENST00000247933.6:c.1469T>C
ENSP00000247933.4:p.Leu490Pro
ENST00000502829.1:n.271T>C

Variation displays