| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000614924 |
| Start |
44529466:44529466(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.44T>C |
| AA Mutation |
p.Leu15Pro(p.L15P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000614924 |
| Start |
44524117:44524117(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.341T>C |
| AA Mutation |
p.Met114Thr(p.M114T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000614924 |
| Start |
44522656:44522656(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.729T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |