Gene >> FOXQ1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000296839 |
| Start |
1313149:1313149(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.445C>T |
| AA Mutation |
p.Leu149Phe(p.L149F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
inframe_deletion |
| Transcription ID |
ENST00000296839 |
| Start |
1313277:1313291(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.577_591delTACTGGATGCTCAAC |
| AA Mutation |
p.Tyr193_Asn197del(p.Y193_N197del) |
| Mutation Classification |
In_Frame_Del |
| Feature Type |
Transcript |