| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000292427 |
| Start |
142879623:142879623(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.191T>A |
| AA Mutation |
p.Leu64Gln(p.L64Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000292427 |
| Start |
142875872:142875872(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.961T>A |
| AA Mutation |
p.Phe321Ile(p.F321I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000292427 |
| Start |
142879752:142879752(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.62C>T |
| AA Mutation |
p.Ala21Val(p.A21V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |