| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000241356 |
| Start |
111500189:111500189(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.718G>A |
| AA Mutation |
p.Ala240Thr(p.A240T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000241356 |
| Start |
111503071:111503071(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.284A>T |
| AA Mutation |
p.His95Leu(p.H95L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000241356 |
| Start |
111500136:111500136(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.771T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |