| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000282478 |
| Start |
87613241:87613241(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1055G>T |
| AA Mutation |
p.Ser352Ile(p.S352I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000282478 |
| Start |
87613976:87613976(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1314C>A |
| AA Mutation |
p.His438Gln(p.H438Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000282478 |
| Start |
87614110:87614110(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1448A>G |
| AA Mutation |
p.Asn483Ser(p.N483S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |