| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000305883 |
| Start |
10048026:10048026(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.689C>G |
| AA Mutation |
p.Ser230Cys(p.S230C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000305883 |
| Start |
10052502:10052502(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1534G>A |
| AA Mutation |
p.Ala512Thr(p.A512T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000305883 |
| Start |
10048027:10048027(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs777257289
|
| CDS Mutation |
c.690C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |