| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000312960 |
| Start |
150742571:150742571(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.545A>G |
| AA Mutation |
p.Glu182Gly(p.E182G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000312960 |
| Start |
150742302:150742302(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.814C>T |
| AA Mutation |
p.Arg272Trp(p.R272W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000312960 |
| Start |
150742627:150742627(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.489C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |