Variant "SLC22A17:c.*1288G>A"
Search result: 1 record
Variant information
Gene:
Variant:
SLC22A17:c.*1288G>A
Genomic location:
chr14:23814569(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_020372.3:c.*1288G>A |
protein_coding | NM_001289050.1:c.*1288G>A |
protein_coding | NM_016609.4:c.*1288G>A |
pseudogene | NR_110290.1:n.*951G>A |
BCL2L2-PABPN1-SLC22A17:n.23814569C>T |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Risk factor(1)
Detail: