| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000308874 |
| Start |
136670319:136670319(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.560C>A |
| AA Mutation |
p.Pro187His(p.P187H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000308874 |
| Start |
136671998:136671998(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.709G>C |
| AA Mutation |
p.Gly237Arg(p.G237R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000308874 |
| Start |
136670320:136670320(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.561C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |