| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000378823 |
| Start |
132603481:132603481(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2389A>G |
| AA Mutation |
p.Arg797Gly(p.R797G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000378823 |
| Start |
132603424:132603424(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2332A>G |
| AA Mutation |
p.Ile778Val(p.I778V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000378823 |
| Start |
132557331:132557331(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.7C>G |
| AA Mutation |
p.Arg3Gly(p.R3G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |