| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000229135 |
| Start |
68158090:68158090(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.189T>A |
| AA Mutation |
p.Ser63Arg(p.S63R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000229135 |
| Start |
68158072:68158072(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.207G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000229135 |
| Start |
68159547:68159547(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.69C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |