| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000324071 |
| Start |
41010052:41010052(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.881C>T |
| AA Mutation |
p.Ser294Leu(p.S294L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000324071 |
| Start |
41016674:41016674(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs143488417
|
| CDS Mutation |
c.1323C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000324071 |
| Start |
41004141:41004141(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.312C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |