| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256412 |
| Start |
24401988:24401988(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1216A>G |
| AA Mutation |
p.Lys406Glu(p.K406E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256412 |
| Start |
24397275:24397275(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.446A>G |
| AA Mutation |
p.Tyr149Cys(p.Y149C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256412 |
| Start |
24398942:24398942(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.831A>G |
| AA Mutation |
p.Ile277Met(p.I277M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |