| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000216341 |
| Start |
24631207:24631207(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.608C>T |
| AA Mutation |
p.Ser203Phe(p.S203F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000216341 |
| Start |
24633033:24633033(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.85C>G |
| AA Mutation |
p.Pro29Ala(p.P29A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000216341 |
| Start |
24632411:24632411(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs747427440
|
| CDS Mutation |
c.252G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |