Gene >> BTRC
| ID |
1 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000370187 |
| Start |
101526013:101526013(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.557C>A |
| AA Mutation |
p.Ala186Asp(p.A186D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000370187 |
| Start |
101479394:101479394(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.261C>G |
| AA Mutation |
p.Cys87Trp(p.C87W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |