| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263817 |
| Start |
168971950:168971950(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1535T>C |
| AA Mutation |
p.Ile512Thr(p.I512T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263817 |
| Start |
168990852:168990852(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.857C>T |
| AA Mutation |
p.Ser286Leu(p.S286L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000263817 |
| Start |
168935204:168935204(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3036C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |