| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000296591 |
| Start |
84106819:84106819(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs781690362
|
| CDS Mutation |
c.481C>A |
| AA Mutation |
p.Pro161Thr(p.P161T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000296591 |
| Start |
83943542:83943542(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1320C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000296591 |
| Start |
84137335:84137335(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.375T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |