| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368636 |
| Start |
131973114:131973114(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.202C>T |
| AA Mutation |
p.Pro68Ser(p.P68S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368636 |
| Start |
131970756:131970756(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.421G>A |
| AA Mutation |
p.Ala141Thr(p.A141T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000368636 |
| Start |
131973939:131973939(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.51C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |