| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000257497 |
| Start |
73160831:73160831(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.413T>G |
| AA Mutation |
p.Ile138Ser(p.I138S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000257497 |
| Start |
73160303:73160303(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.311T>C |
| AA Mutation |
p.Leu104Pro(p.L104P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000257497 |
| Start |
73160822:73160822(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.404A>T |
| AA Mutation |
p.Asp135Val(p.D135V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |