| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000490131 |
| Start |
122284086:122284086(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2132C>T |
| AA Mutation |
p.Pro711Leu(p.P711L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000490131 |
| Start |
122283999:122283999(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2045C>T |
| AA Mutation |
p.Pro682Leu(p.P682L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000490131 |
| Start |
122284321:122284321(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2367C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |