| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265113 |
| Start |
36629485:36629485(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.217A>G |
| AA Mutation |
p.Met73Val(p.M73V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265113 |
| Start |
36683971:36683971(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs763798684
|
| CDS Mutation |
c.1397C>T |
| AA Mutation |
p.Thr466Met(p.T466M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265113 |
| Start |
36629531:36629531(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.263T>C |
| AA Mutation |
p.Leu88Pro(p.L88P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |