| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000328914 |
| Start |
4759488:4759488(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1589C>T |
| AA Mutation |
p.Thr530Ile(p.T530I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000328914 |
| Start |
4759330:4759330(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1431G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000328914 |
| Start |
4761236:4761236(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1869C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |