| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000295902 |
| Start |
64099168:64099168(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2418C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000295902 |
| Start |
64153300:64153300(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.669C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000295902 |
| Start |
64099881:64099881(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1705C>T |
| AA Mutation |
p.Arg569Ter(p.R569*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |