N7D (c.19A>003eG) 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 N7D (c.19A>003eG)

别名

ASN7ASP,C.19A>003eG,RS1311403806
Allele Registry ID：CA351747044
ClinVar ID：

突变位点

Ref. Build: GRCh37 Ensembl Version: 75

Chr.	Start	Stop	Ref. s	Var. Bases
3	10183550	10183550	A	G
Transcript
ENST00000256474.2

基因序列

NC_000003.11:g.10183550A>003eG
NM_000551.3:c.19A>003eG
ENST00000256474.2:c.19A>003eG
NP_000542.1:c.Asn7Asp