| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000296088 |
| Start |
43347874:43347874(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1615A>G |
| AA Mutation |
p.Ser539Gly(p.S539G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000296088 |
| Start |
43340423:43340423(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.868C>G |
| AA Mutation |
p.Leu290Val(p.L290V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000296088 |
| Start |
43347414:43347414(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs766398727
|
| CDS Mutation |
c.1155G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |