Gene >> IFT88
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000319980 |
| Start |
20631055:20631055(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1366A>G |
| AA Mutation |
p.Arg456Gly(p.R456G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000319980 |
| Start |
20638431:20638431(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1513G>A |
| AA Mutation |
p.Ala505Thr(p.A505T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |