| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261799 |
| Start |
150120057:150120057(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2653G>A |
| AA Mutation |
p.Asp885Asn(p.D885N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261799 |
| Start |
150124786:150124786(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs139554380
|
| CDS Mutation |
c.1853C>T |
| AA Mutation |
p.Thr618Met(p.T618M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000261799 |
| Start |
150133752:150133752(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.768G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |