| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000295095 |
| Start |
143216437:143216437(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.288G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000295095 |
| Start |
143768037:143768037(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1293G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000295095 |
| Start |
143228618:143228618(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.334C>T |
| AA Mutation |
p.Arg112Ter(p.R112*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |