| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000269385 |
| Start |
79795203:79795203(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.602C>T |
| AA Mutation |
p.Pro201Leu(p.P201L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000269385 |
| Start |
79795113:79795113(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.692T>C |
| AA Mutation |
p.Leu231Pro(p.L231P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000269385 |
| Start |
79796523:79796523(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.87C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |