| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000369887 |
| Start |
102837279:102837279(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.83C>A |
| AA Mutation |
p.Pro28His(p.P28H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000369887 |
| Start |
102835345:102835345(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.345T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000369887 |
| Start |
102835327:102835327(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.363G>A |
| AA Mutation |
p.Trp121Ter(p.W121*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |