| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000383807 |
| Start |
10064423:10064423(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs754258198
|
| CDS Mutation |
c.2015C>T |
| AA Mutation |
p.Pro672Leu(p.P672L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000383807 |
| Start |
10065937:10065937(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2343C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000383807 |
| Start |
10065457:10065457(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2232G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |