| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000296849 |
| Start |
1032179:1032179(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.169G>C |
| AA Mutation |
p.Gly57Arg(p.G57R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000296849 |
| Start |
1033424:1033424(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.255C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000296849 |
| Start |
1034836:1034836(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.507C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |