| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265333 |
| Start |
133975945:133975945(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.628T>C |
| AA Mutation |
p.Trp210Arg(p.W210R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265333 |
| Start |
133992348:133992348(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.75C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265333 |
| Start |
133975922:133975922(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs542220207
|
| CDS Mutation |
c.651G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |