| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000303924 |
| Start |
121615017:121615017(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.751T>A |
| AA Mutation |
p.Trp251Arg(p.W251R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000303924 |
| Start |
121628837:121628837(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.504G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000303924 |
| Start |
121614832:121614832(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.936T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |