| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000255465 |
| Start |
36438093:36438093(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.571C>A |
| AA Mutation |
p.Leu191Ile(p.L191I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000255465 |
| Start |
36440154:36440154(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1069G>A |
| AA Mutation |
p.Val357Met(p.V357M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000255465 |
| Start |
36438652:36438652(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.678C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |