| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261205 |
| Start |
79217656:79217656(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.137A>C |
| AA Mutation |
p.Lys46Thr(p.K46T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261205 |
| Start |
79285793:79285793(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.173C>T |
| AA Mutation |
p.Pro58Leu(p.P58L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261205 |
| Start |
79296196:79296196(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.602A>T |
| AA Mutation |
p.Lys201Ile(p.K201I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |