| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000298687 |
| Start |
21019733:21019733(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.622T>C |
| AA Mutation |
p.Ser208Pro(p.S208P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000298687 |
| Start |
21022126:21022126(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.280A>C |
| AA Mutation |
p.Asn94His(p.N94H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000298687 |
| Start |
21018027:21018027(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.909G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |