| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000406487 |
| Start |
43071858:43071858(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.806C>T |
| AA Mutation |
p.Ala269Val(p.A269V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000406487 |
| Start |
43075375:43075375(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.688C>G |
| AA Mutation |
p.Pro230Ala(p.P230A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000406487 |
| Start |
43071923:43071923(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.741A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |