| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000242261 |
| Start |
19116850:19116850(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.472T>G |
| AA Mutation |
p.Phe158Val(p.F158V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000242261 |
| Start |
19116822:19116822(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.500A>C |
| AA Mutation |
p.Glu167Ala(p.E167A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000242261 |
| Start |
19116911:19116911(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.411G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |