| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000311772 |
| Start |
27850147:27850147(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.757C>T |
| AA Mutation |
p.Arg253Cys(p.R253C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000311772 |
| Start |
27850099:27850099(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.709C>T |
| AA Mutation |
p.Arg237Cys(p.R237C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000311772 |
| Start |
27838803:27838803(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.222T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |