| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262426 |
| Start |
86510963:86510963(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.394T>C |
| AA Mutation |
p.Phe132Leu(p.F132L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262426 |
| Start |
86511031:86511031(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.462G>T |
| AA Mutation |
p.Met154Ile(p.M154I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262426 |
| Start |
86511472:86511472(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.903C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |