Variant "CDKN2A:c.199G>C(p.Gly67Arg)"
Search result: 1 record
Variant information
Gene:
Variant:
CDKN2A:c.199G>C(p.Gly67Arg)
Genomic location:
chr9:21971159(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_001195132.1:c.199G>C(p.Gly67Arg) |
protein_coding | NM_000077.4:c.199G>C(p.Gly67Arg) |
protein_coding | NM_058195.3:c.242G>C(p.Arg81Pro) |
protein_coding | NM_058197.4:c.*122G>C |
pseudogene | NR_024274.1:n.*3406C>G |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Penetrance(1)
Modifier effect:
Prevention of disease(1)
Detail: