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WormBase Tree Display for Variation: WBVar02004940

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Name Class

WBVar02004940NamePublic_nameWBVar02004940
Other_namecewivar00732532
T28F12.2f.1:c.123+224_123+225insA
T28F12.2d.2:c.-1243+224_-1243+225insA
T28F12.2a.1:c.123+224_123+225insA
T28F12.2c.1:c.-1807+224_-1807+225insA
T28F12.2d.1:c.-1225+224_-1225+225insA
HGVSgCHROMOSOME_V:g.4497813_4497814insA
Sequence_detailsSMapS_parentSequenceT28F12
Flanking_sequencesTCTGAAACTTCAAAACTTTTGGAATTTCGGAAAAAAAAATGAAAAAAATGTTCAAAATGA
Mapping_targetT28F12
Source_location225CHROMOSOME_V44977994497800From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006796
TranscriptT28F12.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT28F12.2c.1:c.-1807+224_-1807+225insA
Intron_number1/10
T28F12.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT28F12.2d.1:c.-1225+224_-1225+225insA
Intron_number1/11
T28F12.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT28F12.2a.1:c.123+224_123+225insA
Intron_number2/11
T28F12.2d.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT28F12.2d.2:c.-1243+224_-1243+225insA
Intron_number1/11
T28F12.2f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT28F12.2f.1:c.123+224_123+225insA
Intron_number2/10
MethodWGS_Flibotte