| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256178 |
| Start |
10568523:10568523(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.10T>G |
| AA Mutation |
p.Cys4Gly(p.C4G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256178 |
| Start |
10568524:10568524(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.9G>T |
| AA Mutation |
p.Arg3Ser(p.R3S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000256178 |
| Start |
10564016:10564016(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.321G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |