| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000370508 |
| Start |
99420722:99420722(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.202A>C |
| AA Mutation |
p.Asn68His(p.N68H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000370508 |
| Start |
99430489:99430489(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.77G>T |
| AA Mutation |
p.Arg26Met(p.R26M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000370508 |
| Start |
99406773:99406773(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.377G>T |
| AA Mutation |
p.Gly126Val(p.G126V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |