| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000334444 |
| Start |
183925622:183925622(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4145T>C |
| AA Mutation |
p.Leu1382Pro(p.L1382P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000334444 |
| Start |
183950046:183950046(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3024A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000334444 |
| Start |
183949986:183949986(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3084G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |