| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356840 |
| Start |
16144937:16144937(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.868C>A |
| AA Mutation |
p.Arg290Ser(p.R290S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000356840 |
| Start |
16145074:16145074(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1005T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000356840 |
| Start |
16143116:16143116(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.561A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |