| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000376285 |
| Start |
100209428:100209428(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.565G>T |
| AA Mutation |
p.Val189Phe(p.V189F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000376285 |
| Start |
100112056:100112056(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.295A>G |
| AA Mutation |
p.Ser99Gly(p.S99G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000376285 |
| Start |
100273218:100273218(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.937C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |