| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360997 |
| Start |
58566605:58566605(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs565978154
|
| CDS Mutation |
c.418G>A |
| AA Mutation |
p.Glu140Lys(p.E140K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000360997 |
| Start |
58569747:58569747(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.114G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000360997 |
| Start |
58569828:58569828(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.33C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |