| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261646 |
| Start |
17818326:17818326(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1117C>G |
| AA Mutation |
p.Leu373Val(p.L373V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261646 |
| Start |
17814729:17814729(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2621A>T |
| AA Mutation |
p.Lys874Met(p.K874M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000261646 |
| Start |
17816494:17816494(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs776609977
|
| CDS Mutation |
c.2010C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |