| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261402 |
| Start |
106066830:106066830(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs757681052
|
| CDS Mutation |
c.1958C>T |
| AA Mutation |
p.Ala653Val(p.A653V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261402 |
| Start |
106138430:106138430(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.224G>T |
| AA Mutation |
p.Arg75Met(p.R75M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000261402 |
| Start |
106067849:106067849(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs143829749
|
| CDS Mutation |
c.939C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |