| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260766 |
| Start |
94306635:94306635(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.5831A>G |
| AA Mutation |
p.Asn1944Ser(p.N1944S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000260766 |
| Start |
94032003:94032003(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.957G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000260766 |
| Start |
94324569:94324569(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.6720+2T>C |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |