Variant "NFATC1:c.2251T>G(p.Cys751Gly)"
Search result: 1 record
Variant information
Gene:
Variant:
NFATC1:c.2251T>G(p.Cys751Gly)
Genomic location:
chr18:77246406(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_001278669.1:c.2251T>G(p.Cys751Gly) |
protein_coding | NM_006162.4:c.2251T>G(p.Cys751Gly) |
protein_coding | NM_172387.2:c.2212T>G(p.Cys738Gly) |
protein_coding | NM_172389.2:c.2212T>G(p.Cys738Gly) |
protein_coding | NM_172388.2:c.835T>G(p.Cys279Gly) |
show all |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Altered onset time(1)
Detail: