| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264832 |
| Start |
10274816:10274816(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs756786973
|
| CDS Mutation |
c.119G>A |
| AA Mutation |
p.Arg40Gln(p.R40Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000264832 |
| Start |
10284551:10284551(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1074G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000264832 |
| Start |
10284208:10284208(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs200759542
|
| CDS Mutation |
c.813G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |