| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262710 |
| Start |
23059438:23059438(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3736A>C |
| AA Mutation |
p.Lys1246Gln(p.K1246Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262710 |
| Start |
23059308:23059308(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3866G>T |
| AA Mutation |
p.Arg1289Met(p.R1289M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262710 |
| Start |
23059363:23059363(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3811C>T |
| AA Mutation |
p.Arg1271Trp(p.R1271W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |