Gene >> MYLIP
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356840 |
| Start |
16130744:16130744(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.275C>T |
| AA Mutation |
p.Thr92Ile(p.T92I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000356840 |
| Start |
16129334:16129334(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.12T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |