| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000377698 |
| Start |
38397144:38397144(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1396G>C |
| AA Mutation |
p.Gly466Arg(p.G466R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000377698 |
| Start |
38396050:38396050(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.302G>T |
| AA Mutation |
p.Arg101Leu(p.R101L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000377698 |
| Start |
38396816:38396816(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1068C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |