| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000315872 |
| Start |
11208321:11208321(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2330A>T |
| AA Mutation |
p.Glu777Val(p.E777V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000315872 |
| Start |
11200975:11200975(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2892A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
splice_acceptor_variant |
| Transcription ID |
ENST00000315872 |
| Start |
11197350:11197350(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3280-2A>T |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |