| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000510508 |
| Start |
101561782:101561782(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.286G>A |
| AA Mutation |
p.Asp96Asn(p.D96N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000510508 |
| Start |
101561992:101561992(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.496G>A |
| AA Mutation |
p.Gly166Ser(p.G166S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000510508 |
| Start |
101562275:101562275(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs538885762
|
| CDS Mutation |
c.779G>A |
| AA Mutation |
p.Arg260His(p.R260H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |