| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000377844 |
| Start |
69719454:69719454(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1930A>G |
| AA Mutation |
p.Thr644Ala(p.T644A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000377844 |
| Start |
69961372:69961372(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.753G>C |
| AA Mutation |
p.Glu251Asp(p.E251D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000377844 |
| Start |
69961339:69961339(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.786T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |