| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000314032 |
| Start |
74003921:74003921(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs779791876
|
| CDS Mutation |
c.730C>T |
| AA Mutation |
p.Arg244Trp(p.R244W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000314032 |
| Start |
74006989:74006989(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.54G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000314032 |
| Start |
74001454:74001454(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.897G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |