| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263087 |
| Start |
3757789:3757789(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.937G>T |
| AA Mutation |
p.Gly313Cys(p.G313C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263087 |
| Start |
3729533:3729533(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2857G>T |
| AA Mutation |
p.Ala953Ser(p.A953S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263087 |
| Start |
3743574:3743574(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2363G>A |
| AA Mutation |
p.Ser788Asn(p.S788N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |