| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356657 |
| Start |
155319642:155319642(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.878A>G |
| AA Mutation |
p.Asn293Ser(p.N293S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356657 |
| Start |
155320556:155320556(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1207C>A |
| AA Mutation |
p.Pro403Thr(p.P403T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000356657 |
| Start |
155318676:155318676(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.696G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |