| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000175506 |
| Start |
97869111:97869111(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.46G>C |
| AA Mutation |
p.Val16Leu(p.V16L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000175506 |
| Start |
97853200:97853200(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs749209281
|
| CDS Mutation |
c.1336C>T |
| AA Mutation |
p.His446Tyr(p.H446Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000175506 |
| Start |
97855398:97855398(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1092A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |