| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000305476 |
| Start |
96864321:96864321(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1024G>C |
| AA Mutation |
p.Glu342Gln(p.E342Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000305476 |
| Start |
96865891:96865891(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.297T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000305476 |
| Start |
96864803:96864803(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs141614070
|
| CDS Mutation |
c.864G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |