| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265403 |
| Start |
68830711:68830711(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1419A>T |
| AA Mutation |
p.Lys473Asn(p.K473N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265403 |
| Start |
68816377:68816377(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.358G>C |
| AA Mutation |
p.Asp120His(p.D120H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265403 |
| Start |
68816224:68816224(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.205T>A |
| AA Mutation |
p.Ser69Thr(p.S69T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |