Gene >> CCNE2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000308108 |
| Start |
94887947:94887947(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.580T>C |
| AA Mutation |
p.Phe194Leu(p.F194L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000308108 |
| Start |
94893925:94893925(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.131A>T |
| AA Mutation |
p.Glu44Val(p.E44V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |