Gene >> HSPA8
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000227378 |
| Start |
123059680:123059680(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.913C>A |
| AA Mutation |
p.Leu305Met(p.L305M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000227378 |
| Start |
123060786:123060786(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.218T>C |
| AA Mutation |
p.Leu73Pro(p.L73P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |