| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000336180 |
| Start |
74111652:74111652(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1289G>C |
| AA Mutation |
p.Ser430Thr(p.S430T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000336180 |
| Start |
74106124:74106124(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs114886936
|
| CDS Mutation |
c.762C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000336180 |
| Start |
74107109:74107109(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.981C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |