| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000251645 |
| Start |
41395303:41395303(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.818T>A |
| AA Mutation |
p.Ile273Asn(p.I273N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000251645 |
| Start |
41397515:41397515(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.25A>T |
| AA Mutation |
p.Ser9Cys(p.S9C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000251645 |
| Start |
41394162:41394162(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1105A>T |
| AA Mutation |
p.Ser369Cys(p.S369C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |