| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361640 |
| Start |
19285956:19285956(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.439G>T |
| AA Mutation |
p.Ala147Ser(p.A147S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361640 |
| Start |
19286263:19286263(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.324C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361640 |
| Start |
19286227:19286227(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs141897650
|
| CDS Mutation |
c.360G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |