| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000246662 |
| Start |
41570206:41570206(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.657A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000246662 |
| Start |
41571762:41571762(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.231T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000246662 |
| Start |
41567740:41567740(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1405G>T |
| AA Mutation |
p.Gly469Ter(p.G469*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |