| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361099 |
| Start |
191009037:191009037(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.199C>A |
| AA Mutation |
p.Gln67Lys(p.Q67K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361099 |
| Start |
191009069:191009069(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.167G>A |
| AA Mutation |
p.Arg56His(p.R56H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361099 |
| Start |
191009005:191009005(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.231C>A |
| AA Mutation |
p.Phe77Leu(p.F77L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |