| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000254351 |
| Start |
20204090:20204090(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.350G>T |
| AA Mutation |
p.Arg117Leu(p.R117L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000254351 |
| Start |
20203190:20203190(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.660G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000254351 |
| Start |
20204008:20204008(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.432G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |