| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000619012 |
| Start |
142866600:142866600(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1582G>A |
| AA Mutation |
p.Asp528Asn(p.D528N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000619012 |
| Start |
142865596:142865596(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1071G>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000619012 |
| Start |
142865620:142865620(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1095C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |