| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000320354 |
| Start |
86567535:86567535(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.200C>A |
| AA Mutation |
p.Pro67His(p.P67H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000320354 |
| Start |
86567625:86567625(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.290G>A |
| AA Mutation |
p.Gly97Asp(p.G97D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000320354 |
| Start |
86568592:86568592(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1257G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |