| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368655 |
| Start |
153818858:153818858(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.530A>C |
| AA Mutation |
p.Glu177Ala(p.E177A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000368655 |
| Start |
153828318:153828318(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.30C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000368655 |
| Start |
153828126:153828126(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.222C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |