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WormBase Tree Display for Variation: WBVar01869503

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Name Class

WBVar01869503NamePublic_nameWBVar01869503
Other_namecewivar00583592
M04G12.1h.1:c.222-139A>G
M04G12.1f.1:c.252-139A>G
M04G12.1c.1:c.222-139A>G
M04G12.1a.1:c.333-139A>G
M04G12.1g.1:c.333-139A>G
M04G12.1b.1:c.252-139A>G
HGVSgCHROMOSOME_V:g.13372367T>C
Sequence_detailsSMapS_parentSequenceM04G12
Flanking_sequencesCGGCAGAAAAATCGTCAAAAAAATATGTTCTTTTCTAATTTTTTTCAAAAAAAAAATTCT
Mapping_targetM04G12
Source_location225CHROMOSOME_V1337235413372354From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00010867
TranscriptM04G12.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM04G12.1g.1:c.333-139A>G
Intron_number1/5
M04G12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM04G12.1a.1:c.333-139A>G
Intron_number2/7
M04G12.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM04G12.1h.1:c.222-139A>G
Intron_number1/4
M04G12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM04G12.1b.1:c.252-139A>G
Intron_number3/7
M04G12.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM04G12.1f.1:c.252-139A>G
Intron_number2/6
M04G12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM04G12.1c.1:c.222-139A>G
Intron_number1/5
MethodWGS_Flibotte