| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356876 |
| Start |
6464672:6464672(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.343T>A |
| AA Mutation |
p.Cys115Ser(p.C115S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356876 |
| Start |
6462144:6462144(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.775C>T |
| AA Mutation |
p.His259Tyr(p.H259Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000356876 |
| Start |
6464670:6464670(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.345T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |