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WormBase Tree Display for Variation: WBVar02100998

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Name Class

WBVar02100998NamePublic_nameWBVar02100998
Other_namecewivar00831237
H10E21.3b.1:c.41_64delinsATCAAAATTCCAACTTT
CE19488:p.Thr14AsnfsTer16
H10E21.3a.1:c.14-27_14-4delinsATCAAAATTCCAACTTT
HGVSgCHROMOSOME_III:g.14690_14713delinsAAAGTTGGAATTTTGAT
Sequence_detailsSMapS_parentSequenceH10E21
Flanking_sequencesTTAGACATCGCGTGGAGCTGGAAGAAGCTGTTTTTTTTCTAATTTCCAAATACCTACCTT
Mapping_targetH10E21
Source_location225CHROMOSOME_III1469014713From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionAAAGTTGGAATTTTGAT
Deletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00003670
TranscriptH10E21.3b.1VEP_consequenceframeshift_variant
VEP_impactHIGH
HGVScH10E21.3b.1:c.41_64delinsATCAAAATTCCAACTTT
HGVSpCE19488:p.Thr14AsnfsTer16
cDNA_position41-64
CDS_position41-64
Protein_position14-22
Exon_number1/7
Codon_changeaCTGTAAAATCAAAATTCCGATTTCca/aATCAAAATTCCAACTTTca
Amino_acid_changeTVKSKFRFP/NQNSNFX
H10E21.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH10E21.3a.1:c.14-27_14-4delinsATCAAAATTCCAACTTT
Intron_number2/8
MethodWGS_Flibotte