| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000278070 |
| Start |
102148866:102148866(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs370946381
|
| CDS Mutation |
c.4667G>A |
| AA Mutation |
p.Arg1556Gln(p.R1556Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000278070 |
| Start |
102147267:102147267(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4275C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000278070 |
| Start |
102141262:102141262(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2754C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |