Variant "SCN5A:c.1535C>T(p.Thr512Ile)"
Search result: 1 record
Variant information
Gene:
Variant:
SCN5A:c.1535C>T(p.Thr512Ile)
Genomic location:
chr3:38645558(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_001099404.1:c.1535C>T(p.Thr512Ile) |
protein_coding | NM_000335.4:c.1535C>T(p.Thr512Ile) |
protein_coding | NM_001099405.1:c.1535C>T(p.Thr512Ile) |
protein_coding | NM_198056.2:c.1535C>T(p.Thr512Ile) |
protein_coding | NM_001160160.1:c.1535C>T(p.Thr512Ile) |
show all |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Altered severity(1)
Detail: