| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256720 |
| Start |
11771565:11771565(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.482A>G |
| AA Mutation |
p.Lys161Arg(p.K161R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256720 |
| Start |
11773649:11773649(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.626A>T |
| AA Mutation |
p.Gln209Leu(p.Q209L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000256720 |
| Start |
11771488:11771488(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.405G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |