Gene >> WWP2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000359154 |
| Start |
69840204:69840204(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.419T>A |
| AA Mutation |
p.Phe140Tyr(p.F140Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000359154 |
| Start |
69799296:69799296(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.340+1G>T |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |