| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000329321 |
| Start |
132417253:132417253(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.211C>A |
| AA Mutation |
p.His71Asn(p.H71N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000329321 |
| Start |
132417855:132417855(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs558356688
|
| CDS Mutation |
c.813C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000329321 |
| Start |
132645417:132645417(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs761843800
|
| CDS Mutation |
c.1173G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |