| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368712 |
| Start |
153547699:153547699(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs571596892
|
| CDS Mutation |
c.289C>T |
| AA Mutation |
p.Pro97Ser(p.P97S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368712 |
| Start |
153548391:153548391(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs770094114
|
| CDS Mutation |
c.95C>T |
| AA Mutation |
p.Ala32Val(p.A32V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000368712 |
| Start |
153547763:153547763(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.225T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |