| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000330899 |
| Start |
33030487:33030487(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.463G>T |
| AA Mutation |
p.Gly155Cys(p.G155C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000330899 |
| Start |
33037065:33037065(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.925C>T |
| AA Mutation |
p.Pro309Ser(p.P309S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000330899 |
| Start |
33030449:33030449(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.425G>A |
| AA Mutation |
p.Gly142Asp(p.G142D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |