| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367182 |
| Start |
204542939:204542939(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.667A>G |
| AA Mutation |
p.Asn223Asp(p.N223D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367182 |
| Start |
204530706:204530706(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.176A>G |
| AA Mutation |
p.Tyr59Cys(p.Y59C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367182 |
| Start |
204537489:204537489(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.403C>A |
| AA Mutation |
p.Gln135Lys(p.Q135K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |