| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000284629 |
| Start |
117363646:117363646(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs766532245
|
| CDS Mutation |
c.1378G>A |
| AA Mutation |
p.Gly460Arg(p.G460R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000284629 |
| Start |
117363716:117363716(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1308T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000284629 |
| Start |
117420207:117420207(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.396A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |