Variant "SCN5A:c.3269C>T(p.Pro1090Leu)"
Search result: 1 record
Variant information
Gene:
Variant:
SCN5A:c.3269C>T(p.Pro1090Leu)
Genomic location:
chr3:38620946(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_001099404.1:c.3269C>T(p.Pro1090Leu) |
protein_coding | NM_001099405.1:c.3269C>T(p.Pro1090Leu) |
protein_coding | NM_198056.2:c.3269C>T(p.Pro1090Leu) |
protein_coding | NM_000335.4:c.3266C>T(p.Pro1089Leu) |
protein_coding | NM_001160160.1:c.3266C>T(p.Pro1089Leu) |
show all |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Risk factor(1)
Detail: