| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000346208 |
| Start |
8064112:8064112(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs774440409
|
| CDS Mutation |
c.895C>A |
| AA Mutation |
p.Pro299Thr(p.P299T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000346208 |
| Start |
8064063:8064063(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs138698611
|
| CDS Mutation |
c.846C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000346208 |
| Start |
8055862:8055862(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.207G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |