| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000617897 |
| Start |
35997819:35997819(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.290G>T |
| AA Mutation |
p.Ser97Ile(p.S97I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000617897 |
| Start |
35998895:35998895(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.107T>G |
| AA Mutation |
p.Leu36Arg(p.L36R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000617897 |
| Start |
35997806:35997806(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.303T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |