| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000334575 |
| Start |
52792896:52792896(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.506A>G |
| AA Mutation |
p.Glu169Gly(p.E169G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000334575 |
| Start |
52796252:52796252(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs530255410
|
| CDS Mutation |
c.202A>G |
| AA Mutation |
p.Thr68Ala(p.T68A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000334575 |
| Start |
52792939:52792939(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.463C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |