| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000337539 |
| Start |
24441137:24441137(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs199792438
|
| CDS Mutation |
c.887G>A |
| AA Mutation |
p.Arg296His(p.R296H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000337539 |
| Start |
24440628:24440628(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.378C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000337539 |
| Start |
24441231:24441231(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.981T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |