| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000355870 |
| Start |
23710313:23710313(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.28G>T |
| AA Mutation |
p.Ala10Ser(p.A10S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000355870 |
| Start |
23735646:23735646(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.592G>A |
| AA Mutation |
p.Asp198Asn(p.D198N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000355870 |
| Start |
23752826:23752826(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1127A>C |
| AA Mutation |
p.Glu376Ala(p.E376A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |