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WormBase Tree Display for Variation: WBVar02067029

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Name Class

WBVar02067029NamePublic_nameWBVar02067029
Other_namecewivar00796280
Y57A10A.18a.2:c.1782+383_1783-380del
Y57A10A.18c.1:c.1792-317_1792-311del
Y57A10A.18a.1:c.1782+383_1783-380del
Y57A10A.18e.1:c.1783-305_1783-299del
Y57A10A.18d.1:c.1851+383_1852-380del
Y57A10A.18b.1:c.1782+383_1783-380del
HGVSgCHROMOSOME_II:g.12215267_12215273del
Sequence_detailsSMapS_parentSequenceY57A10A
Flanking_sequencesATTTTCGAGGCCCCACCAAAACAGGATGCAGGGGGGCGGAGCAAATCCGCAACCACCGCA
Mapping_targetY57A10A
Source_location225CHROMOSOME_II1221520312215209From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
Origin (5)
AffectsGeneWBGene00004167
TranscriptY57A10A.18a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY57A10A.18a.2:c.1782+383_1783-380del
Intron_number11/15
Y57A10A.18c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY57A10A.18c.1:c.1792-317_1792-311del
Intron_number10/14
Y57A10A.18e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY57A10A.18e.1:c.1783-305_1783-299del
Intron_number11/15
Y57A10A.18a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY57A10A.18a.1:c.1782+383_1783-380del
Intron_number12/16
Y57A10A.18d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY57A10A.18d.1:c.1851+383_1852-380del
Intron_number11/15
Y57A10A.18b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY57A10A.18b.1:c.1782+383_1783-380del
Intron_number12/16
MethodWGS_Flibotte