| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000341099 |
| Start |
64280082:64280082(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.434A>G |
| AA Mutation |
p.Asp145Gly(p.D145G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000341099 |
| Start |
64257264:64257264(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs747912769
|
| CDS Mutation |
c.1053C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000341099 |
| Start |
64260495:64260495(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.906C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |