| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000366541 |
| Start |
243271017:243271017(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.260A>C |
| AA Mutation |
p.Lys87Thr(p.K87T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000366541 |
| Start |
243304719:243304719(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.682C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000366541 |
| Start |
243316788:243316788(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs751551796
|
| CDS Mutation |
c.963C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |