| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000322886 |
| Start |
77033973:77033973(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1193A>C |
| AA Mutation |
p.Gln398Pro(p.Q398P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000322886 |
| Start |
77050735:77050735(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.379G>T |
| AA Mutation |
p.Val127Phe(p.V127F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000322886 |
| Start |
77033085:77033085(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1347A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |