| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000074304 |
| Start |
98555717:98555717(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1746G>T |
| AA Mutation |
p.Trp582Cys(p.W582C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000074304 |
| Start |
98565750:98565750(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2278G>A |
| AA Mutation |
p.Val760Ile(p.V760I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000074304 |
| Start |
98564688:98564688(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2092C>T |
| AA Mutation |
p.His698Tyr(p.H698Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |