| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000285679 |
| Start |
15825046:15825046(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1289A>G |
| AA Mutation |
p.Gln430Arg(p.Q430R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000285679 |
| Start |
15866336:15866336(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2587G>C |
| AA Mutation |
p.Glu863Gln(p.E863Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000285679 |
| Start |
15877885:15877885(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2889C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |