| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000324041 |
| Start |
50907071:50907071(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.628C>G |
| AA Mutation |
p.Pro210Ala(p.P210A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000324041 |
| Start |
50908638:50908638(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.416C>T |
| AA Mutation |
p.Ser139Leu(p.S139L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000324041 |
| Start |
50908673:50908673(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.381C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |