| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263408 |
| Start |
39308239:39308239(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1231G>A |
| AA Mutation |
p.Gly411Ser(p.G411S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263408 |
| Start |
39306781:39306781(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1252A>G |
| AA Mutation |
p.Ser418Gly(p.S418G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263408 |
| Start |
39341627:39341627(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs764410729
|
| CDS Mutation |
c.257G>A |
| AA Mutation |
p.Arg86Gln(p.R86Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |