N78T (c.233A>003eC) 基因突变 VHL癌基因 - 癌症123

基因突变

VHL 突变位点基因序列 VHL N78T (c.233A>003eC)

别名

C.233A>003eC,ASN78THR,RS5030804
Allele Registry ID：CA357095
ClinVar ID：223168

突变位点

Ref. Build: GRCh37 Ensembl Version: 75

Chr.	Start	Stop	Ref. s	Var. Bases
3	10183764	10183764	A	C
Transcript
ENST000

基因序列

NM_000551.3:c.233A>003eC
NP_000542.1:p.Asn78Thr
NC_000003.11:g.10183764A>003eC
ENST00000256474.2:c.233A>003eC