| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000527614 |
| Start |
111752221:111752221(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1276G>C |
| AA Mutation |
p.Asp426His(p.D426H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000527614 |
| Start |
111753473:111753473(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1134A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000527614 |
| Start |
111765358:111765358(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.141A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |