| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000281172 |
| Start |
15650854:15650854(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs748350706
|
| CDS Mutation |
c.1403G>A |
| AA Mutation |
p.Arg468His(p.R468H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000281172 |
| Start |
15654198:15654198(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1197T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000281172 |
| Start |
15654279:15654279(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1116A>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |