| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000312403 |
| Start |
61249766:61249766(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.871G>A |
| AA Mutation |
p.Ala291Thr(p.A291T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000312403 |
| Start |
61249958:61249958(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs145812727
|
| CDS Mutation |
c.961G>A |
| AA Mutation |
p.Val321Ile(p.V321I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000312403 |
| Start |
61249681:61249681(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs139579497
|
| CDS Mutation |
c.786C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |