Gene >> NCR2
| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000373089 |
| Start |
41341909:41341909(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.510T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000373089 |
| Start |
41341886:41341886(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.487A>T |
| AA Mutation |
p.Arg163Ter(p.R163*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |