| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380554 |
| Start |
5102107:5102107(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.577T>C |
| AA Mutation |
p.Cys193Arg(p.C193R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000380554 |
| Start |
5097452:5097452(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.271C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000380554 |
| Start |
5094453:5094453(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.9C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |