| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000327097 |
| Start |
118982386:118982386(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1039C>A |
| AA Mutation |
p.Leu347Met(p.L347M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000327097 |
| Start |
118970186:118970186(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.272G>T |
| AA Mutation |
p.Ser91Ile(p.S91I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000327097 |
| Start |
118942336:118942336(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.36C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |