| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000251808 |
| Start |
101558514:101558514(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.380A>G |
| AA Mutation |
p.Asn127Ser(p.N127S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000251808 |
| Start |
101558601:101558601(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.467C>T |
| AA Mutation |
p.Thr156Met(p.T156M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000251808 |
| Start |
101543410:101543410(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.190C>T |
| AA Mutation |
p.Leu64Phe(p.L64F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |