| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000234798 |
| Start |
1222218:1222218(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs770021673
|
| CDS Mutation |
c.635G>A |
| AA Mutation |
p.Arg212Gln(p.R212Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000234798 |
| Start |
1223479:1223479(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs376013233
|
| CDS Mutation |
c.189C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000234798 |
| Start |
1222025:1222025(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs777443570
|
| CDS Mutation |
c.729T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |