| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000252050 |
| Start |
43215149:43215149(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs773794574
|
| CDS Mutation |
c.5759C>T |
| AA Mutation |
p.Ala1920Val(p.A1920V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000252050 |
| Start |
43184730:43184730(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs146357794
|
| CDS Mutation |
c.420C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000252050 |
| Start |
43187295:43187295(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs148427416
|
| CDS Mutation |
c.1437G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |