| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000255040 |
| Start |
159588233:159588233(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.197A>G |
| AA Mutation |
p.Tyr66Cys(p.Y66C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000255040 |
| Start |
159588235:159588235(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.199A>T |
| AA Mutation |
p.Ser67Cys(p.S67C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000255040 |
| Start |
159588313:159588313(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs771351516
|
| CDS Mutation |
c.277T>C |
| AA Mutation |
p.Tyr93His(p.Y93H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |