| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000528429 |
| Start |
16183932:16183932(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.731T>C |
| AA Mutation |
p.Leu244Pro(p.L244P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000528429 |
| Start |
15973094:15973094(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2202A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000528429 |
| Start |
16055836:16055836(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs774229287
|
| CDS Mutation |
c.1167A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |