| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000345146 |
| Start |
208248389:208248389(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs121913499
|
| CDS Mutation |
c.394C>A |
| AA Mutation |
p.Arg132Ser(p.R132S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000345146 |
| Start |
208248415:208248415(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.368G>A |
| AA Mutation |
p.Gly123Glu(p.G123E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000345146 |
| Start |
208248389:208248389(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs121913499
|
| CDS Mutation |
c.394C>T |
| AA Mutation |
p.Arg132Cys(p.R132C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |