| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000381125 |
| Start |
3108782:3108782(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs776455980
|
| CDS Mutation |
c.952G>A |
| AA Mutation |
p.Asp318Asn(p.D318N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000381125 |
| Start |
3103892:3103892(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.568G>A |
| AA Mutation |
p.Ala190Thr(p.A190T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000381125 |
| Start |
3118809:3118809(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1470G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |