| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260197 |
| Start |
121513091:121513091(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1028G>T |
| AA Mutation |
p.Arg343Ile(p.R343I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260197 |
| Start |
121589264:121589264(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3952G>T |
| AA Mutation |
p.Asp1318Tyr(p.D1318Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000260197 |
| Start |
121570179:121570179(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3246G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |