Gene >> TSPYL5
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000322128 |
| Start |
97277747:97277747(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.98C>T |
| AA Mutation |
p.Pro33Leu(p.P33L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000322128 |
| Start |
97277239:97277239(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.606G>A |
| AA Mutation |
p.Met202Ile(p.M202I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |