| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000375203 |
| Start |
32126180:32126180(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.415G>A |
| AA Mutation |
p.Asp139Asn(p.D139N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000375203 |
| Start |
32128192:32128192(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.16C>A |
| AA Mutation |
p.Leu6Met(p.L6M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000375203 |
| Start |
32127458:32127458(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.234C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |