| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000379775 |
| Start |
6215310:6215310(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.292G>T |
| AA Mutation |
p.Val98Phe(p.V98F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000379775 |
| Start |
6203298:6203298(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.38T>C |
| AA Mutation |
p.Ile13Thr(p.I13T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000379775 |
| Start |
6216771:6216771(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.432T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |