| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000311737 |
| Start |
142752953:142752953(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.677C>T |
| AA Mutation |
p.Pro226Leu(p.P226L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000311737 |
| Start |
142752552:142752552(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.576C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000311737 |
| Start |
142752459:142752459(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.483G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |