| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000517956 |
| Start |
123503395:123503395(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1046T>C |
| AA Mutation |
p.Phe349Ser(p.F349S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000517956 |
| Start |
123504645:123504645(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.937A>G |
| AA Mutation |
p.Thr313Ala(p.T313A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000517956 |
| Start |
123531935:123531935(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.335C>T |
| AA Mutation |
p.Ala112Val(p.A112V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |