| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000328111 |
| Start |
32792759:32792759(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1055A>C |
| AA Mutation |
p.Asn352Thr(p.N352T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000328111 |
| Start |
32799286:32799286(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs764722946
|
| CDS Mutation |
c.1717C>T |
| AA Mutation |
p.Arg573Trp(p.R573W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000328111 |
| Start |
32797249:32797249(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1440G>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |