| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000282441 |
| Start |
102223686:102223686(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1097C>G |
| AA Mutation |
p.Ser366Cys(p.S366C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000282441 |
| Start |
102227571:102227571(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1266G>C |
| AA Mutation |
p.Glu422Asp(p.E422D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000282441 |
| Start |
102229839:102229839(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1414C>G |
| AA Mutation |
p.Pro472Ala(p.P472A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |