| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000542575 |
| Start |
46778831:46778831(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.902G>A |
| AA Mutation |
p.Arg301His(p.R301H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000542575 |
| Start |
46777293:46777293(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1171G>A |
| AA Mutation |
p.Ala391Thr(p.A391T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000542575 |
| Start |
46777279:46777279(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1185C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |