| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000366999 |
| Start |
211669220:211669220(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.878C>G |
| AA Mutation |
p.Pro293Arg(p.P293R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000366999 |
| Start |
211670292:211670292(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.754T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000366999 |
| Start |
211667104:211667104(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1111+2T>A |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |