| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000366930 |
| Start |
218405264:218405264(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.442G>C |
| AA Mutation |
p.Glu148Gln(p.E148Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000366930 |
| Start |
218435989:218435989(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.774A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000366930 |
| Start |
218435989:218435989(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.774A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |