| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000300738 |
| Start |
4121760:4121760(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1033A>T |
| AA Mutation |
p.Asn345Tyr(p.N345Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000300738 |
| Start |
4138353:4138353(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2349T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000300738 |
| Start |
4127130:4127130(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1566A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |