| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368931 |
| Start |
151046677:151046677(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1064G>C |
| AA Mutation |
p.Gly355Ala(p.G355A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000368931 |
| Start |
151045800:151045800(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs370988337
|
| CDS Mutation |
c.855A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000368931 |
| Start |
151042987:151042987(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.465C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |