| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256078 |
| Start |
25245350:25245350(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs121913529
|
| CDS Mutation |
c.35G>A |
| AA Mutation |
p.Gly12Asp(p.G12D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256078 |
| Start |
25245347:25245347(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs112445441
|
| CDS Mutation |
c.38G>A |
| AA Mutation |
p.Gly13Asp(p.G13D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256078 |
| Start |
25227321:25227321(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.203G>T |
| AA Mutation |
p.Arg68Met(p.R68M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |