| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000399799 |
| Start |
20967889:20967889(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3055A>G |
| AA Mutation |
p.Arg1019Gly(p.R1019G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000399799 |
| Start |
20979952:20979952(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2612A>C |
| AA Mutation |
p.Asn871Thr(p.N871T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000399799 |
| Start |
21042680:21042680(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.705T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |