| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000286639 |
| Start |
75525138:75525138(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.118G>A |
| AA Mutation |
p.Ala40Thr(p.A40T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000286639 |
| Start |
75546544:75546544(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.251C>T |
| AA Mutation |
p.Ser84Leu(p.S84L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000286639 |
| Start |
75546560:75546560(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.267C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |