| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000286574 |
| Start |
65068800:65068800(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.502C>A |
| AA Mutation |
p.Pro168Thr(p.P168T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000286574 |
| Start |
65077823:65077823(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.320G>C |
| AA Mutation |
p.Arg107Pro(p.R107P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000286574 |
| Start |
65067705:65067705(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs762822872
|
| CDS Mutation |
c.624C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |