| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000295542 |
| Start |
155039465:155039465(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.325C>T |
| AA Mutation |
p.Pro109Ser(p.P109S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000295542 |
| Start |
155043461:155043461(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs772085683
|
| CDS Mutation |
c.1124G>A |
| AA Mutation |
p.Gly375Glu(p.G375E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000295542 |
| Start |
155040554:155040554(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.461A>C |
| AA Mutation |
p.Gln154Pro(p.Q154P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |