| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000335327 |
| Start |
26681097:26681097(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.760C>T |
| AA Mutation |
p.Pro254Ser(p.P254S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000335327 |
| Start |
26682732:26682732(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs147802301
|
| CDS Mutation |
c.1109C>T |
| AA Mutation |
p.Pro370Leu(p.P370L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000335327 |
| Start |
26681075:26681075(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs757584113
|
| CDS Mutation |
c.738G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |