| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000220849 |
| Start |
108217357:108217357(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.826G>A |
| AA Mutation |
p.Asp276Asn(p.D276N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000220849 |
| Start |
108239989:108239989(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.292C>T |
| AA Mutation |
p.Pro98Ser(p.P98S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000220849 |
| Start |
108240050:108240050(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.231G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |