| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000326932 |
| Start |
11965834:11965834(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.805A>T |
| AA Mutation |
p.Ser269Cys(p.S269C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000326932 |
| Start |
11965816:11965816(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.823C>T |
| AA Mutation |
p.Pro275Ser(p.P275S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000326932 |
| Start |
11968473:11968473(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.450C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |