| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000274341 |
| Start |
83641653:83641653(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.908G>T |
| AA Mutation |
p.Arg303Leu(p.R303L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000274341 |
| Start |
83644635:83644635(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.503G>T |
| AA Mutation |
p.Gly168Val(p.G168V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000274341 |
| Start |
83644382:83644382(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.756T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |