| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000318066 |
| Start |
93411112:93411112(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.218C>T |
| AA Mutation |
p.Thr73Ile(p.T73I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000318066 |
| Start |
93441881:93441881(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.4G>A |
| AA Mutation |
p.Ala2Thr(p.A2T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000318066 |
| Start |
93410814:93410814(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.338G>C |
| AA Mutation |
p.Ser113Thr(p.S113T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |