| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260731 |
| Start |
92609395:92609395(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.584T>C |
| AA Mutation |
p.Ile195Thr(p.I195T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260731 |
| Start |
92613502:92613502(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.915A>T |
| AA Mutation |
p.Arg305Ser(p.R305S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000260731 |
| Start |
92616784:92616784(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1080G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |