Gene >> SYNM
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000336292 |
| Start |
99129451:99129451(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1091C>A |
| AA Mutation |
p.Pro364His(p.P364H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000336292 |
| Start |
99131377:99131377(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3017C>T |
| AA Mutation |
p.Ser1006Leu(p.S1006L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |