| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265717 |
| Start |
107140935:107140935(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.569A>G |
| AA Mutation |
p.Asn190Ser(p.N190S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265717 |
| Start |
107140950:107140950(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.584A>T |
| AA Mutation |
p.Asp195Val(p.D195V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265717 |
| Start |
107159477:107159477(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1152T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |