| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000375533 |
| Start |
28682178:28682178(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201458451
|
| CDS Mutation |
c.560G>A |
| AA Mutation |
p.Arg187Gln(p.R187Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000375533 |
| Start |
28682377:28682377(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs374748047
|
| CDS Mutation |
c.759G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000375533 |
| Start |
28682249:28682249(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.631T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |