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WormBase Tree Display for Variation: WBVar01691437

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Name Class

WBVar01691437NamePublic_nameWBVar01691437
Other_namecewivar00383537
R12H7.1a.1:c.391+235G>A
R12H7.1b.1:c.199+235G>A
R12H7.1a.2:c.391+235G>A
HGVSgCHROMOSOME_X:g.13213589G>A
Sequence_detailsSMapS_parentSequenceR12H7
Flanking_sequencesTGTTGTTTTCAAGAAAAAAACGAAGAAAAACGTCAAGAACGGCGTGAAGAAGAAGAACAA
Mapping_targetR12H7
Source_location225CHROMOSOME_X1321352013213520From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006749
TranscriptR12H7.1a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR12H7.1a.2:c.391+235G>A
Intron_number6/10
R12H7.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR12H7.1a.1:c.391+235G>A
Intron_number5/9
R12H7.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR12H7.1b.1:c.199+235G>A
Intron_number2/5
MethodWGS_Flibotte