| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263285 |
| Start |
160813794:160813794(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.613T>C |
| AA Mutation |
p.Ser205Pro(p.S205P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263285 |
| Start |
160814675:160814675(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.986T>C |
| AA Mutation |
p.Ile329Thr(p.I329T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000263285 |
| Start |
160814496:160814496(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.807T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |