WormBase Tree Display for Variation: WBVar01451962
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WBVar01451962 | Evidence | Paper_evidence | WBPaper00040707 | ||
---|---|---|---|---|---|
Name | Public_name | WBVar01451962 | |||
Other_name | F56D6.2.1:c.1370+22T>C | ||||
F56D6.2.2:c.1370+22T>C | |||||
HGVSg | CHROMOSOME_IV:g.3924364T>C | ||||
Sequence_details | SMap | S_parent | Sequence | F56D6 | |
Flanking_sequences | CAGCCCATAGTGAGTAGTTTATTTGATGAA | ATAGTTCTAAAAAGCCTTTTTTCAGCGCCACAACCTATTGGTTGCCGTATTCTGATTAAGGACATTGTAA | |||
Mapping_target | F56D6 | ||||
Type_of_mutation | Substitution | t | c | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Natural_variant | |||||
Origin (7) | |||||
Affects | Gene | WBGene00018971 | |||
Transcript | F56D6.2.2 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | F56D6.2.2:c.1370+22T>C | ||||
Intron_number | 9/10 | ||||
F56D6.2.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F56D6.2.1:c.1370+22T>C | ||||
Intron_number | 9/10 | ||||
Reference | WBPaper00040707 | ||||
Method | WGS_Andersen |