| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000232424 |
| Start |
194137010:194137010(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.254T>C |
| AA Mutation |
p.Val85Ala(p.V85A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000232424 |
| Start |
194137856:194137856(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.466C>T |
| AA Mutation |
p.Pro156Ser(p.P156S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000232424 |
| Start |
194136975:194136975(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.219C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |