| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263102 |
| Start |
59793107:59793107(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1235C>T |
| AA Mutation |
p.Pro412Leu(p.P412L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263102 |
| Start |
59812663:59812663(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.819G>T |
| AA Mutation |
p.Lys273Asn(p.K273N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000263102 |
| Start |
59794506:59794506(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs761874280
|
| CDS Mutation |
c.1197C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |