| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000343483 |
| Start |
27163678:27163678(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.744G>C |
| AA Mutation |
p.Arg248Ser(p.R248S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000343483 |
| Start |
27165338:27165338(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.120G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000343483 |
| Start |
27165152:27165152(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.306G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |