| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368195 |
| Start |
156854241:156854241(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs558428940
|
| CDS Mutation |
c.148G>A |
| AA Mutation |
p.Val50Met(p.V50M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368195 |
| Start |
156843451:156843451(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2872C>A |
| AA Mutation |
p.Pro958Thr(p.P958T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000368195 |
| Start |
156849430:156849430(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1260G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |