| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000369784 |
| Start |
110340784:110340784(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1379G>C |
| AA Mutation |
p.Gly460Ala(p.G460A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000369784 |
| Start |
110340105:110340105(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.700G>T |
| AA Mutation |
p.Ala234Ser(p.A234S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000369784 |
| Start |
110340106:110340106(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.701C>T |
| AA Mutation |
p.Ala234Val(p.A234V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |