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WormBase Tree Display for Variation: WBVar01710587

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Name Class

WBVar01710587NamePublic_nameWBVar01710587
Other_namecewivar00408240
C07A12.7b.1:c.586-69T>C
C07A12.7a.1:c.688-69T>C
C07A12.7c.2:c.-204-69T>C
C07A12.7c.1:c.-273T>C
C07A12.7a.2:c.688-69T>C
HGVSgCHROMOSOME_X:g.4518754A>G
Sequence_detailsSMapS_parentSequenceC07A12
Flanking_sequencesAAACAAACAAACTTTGTAATGAAACTTTTCAAATTTTTCAGAAATGTTTCATGACGGTTC
Mapping_targetC07A12
Source_location225CHROMOSOME_X45187264518726From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00022902From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00015561
TranscriptC07A12.7c.1VEP_consequence5_prime_UTR_variant
VEP_impactMODIFIER
HGVScC07A12.7c.1:c.-273T>C
cDNA_position1288
Exon_number4/9
C07A12.7a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC07A12.7a.2:c.688-69T>C
Intron_number6/10
C07A12.7c.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC07A12.7c.2:c.-204-69T>C
Intron_number3/8
C07A12.7b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC07A12.7b.1:c.586-69T>C
Intron_number4/8
C07A12.7a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC07A12.7a.1:c.688-69T>C
Intron_number5/9
MethodWGS_Flibotte