| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000396634 |
| Start |
29942920:29942920(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.237G>T |
| AA Mutation |
p.Glu79Asp(p.E79D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000396634 |
| Start |
29944507:29944507(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.903T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000396634 |
| Start |
29942992:29942992(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.309G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |