| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000337659 |
| Start |
4032705:4032705(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs751880533
|
| CDS Mutation |
c.1188C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000337659 |
| Start |
4032237:4032237(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.720A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000337659 |
| Start |
4060515:4060515(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2923C>T |
| AA Mutation |
p.Gln975Ter(p.Q975*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |