WormBase Tree Display for Variation: WBVar01460797
expand all nodes | collapse all nodes | view schema
WBVar01460797 | Evidence | Paper_evidence | WBPaper00040707 | |||
---|---|---|---|---|---|---|
Name | Public_name | WBVar01460797 | ||||
Other_name | C26F1.3.1:c.421+346T>C | |||||
HGVSg | CHROMOSOME_V:g.7778202T>C | |||||
Sequence_details | SMap | S_parent | Sequence | C26F1 | ||
Flanking_sequences | TACGGCGCTTTGAACACGTTTTAATTTATT | CACCCTTAAAAATGAAGAATTCATCGAAAT | ||||
Mapping_target | C26F1 | |||||
Type_of_mutation | Substitution | t | c | |||
SeqStatus | Sequenced | |||||
Variation_type | SNP | |||||
Natural_variant | ||||||
Origin | Species | Caenorhabditis elegans | ||||
Strain | WBStrain00023071 | From_analysis | WGS_Andersen | |||
Laboratory | QX | |||||
Person | WBPerson1730 | |||||
Analysis | WGS_Andersen | |||||
DB_info | Database | dbSNP_rs | rs | 193346453 | ||
dbSNP_ss | ss | 295522372 | ||||
Status | Live | |||||
Affects | Gene | WBGene00016148 | ||||
Transcript | C26F1.3.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | C26F1.3.1:c.421+346T>C | |||||
Intron_number | 2/3 | |||||
Reference | WBPaper00040707 | |||||
Method | WGS_Andersen |