| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361084 |
| Start |
156070202:156070202(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs61995861
|
| CDS Mutation |
c.557G>A |
| AA Mutation |
p.Arg186Gln(p.R186Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361084 |
| Start |
156070223:156070223(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.578G>A |
| AA Mutation |
p.Gly193Asp(p.G193D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361084 |
| Start |
156066041:156066041(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201223792
|
| CDS Mutation |
c.174C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |