| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360906 |
| Start |
32241051:32241051(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2332G>C |
| AA Mutation |
p.Glu778Gln(p.E778Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360906 |
| Start |
32251037:32251037(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.827T>A |
| AA Mutation |
p.Ile276Asn(p.I276N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000360906 |
| Start |
32238136:32238136(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2517C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |