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WormBase Tree Display for Variation: WBVar01690638

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Name Class

WBVar01690638NamePublic_nameWBVar01690638
Other_namecewivar00382692
C34E11.2f.1:c.1713+158G>T
C34E11.2e.1:c.1995+158G>T
C34E11.2d.1:c.1670+158G>T
C34E11.2g.1:c.1627+158G>T
C34E11.2a.1:c.1952+158G>T
C34E11.2c.1:c.1853+158G>T
C34E11.2b.1:c.1685+158G>T
HGVSgCHROMOSOME_X:g.11807172C>A
Sequence_detailsSMapS_parentSequenceC34E11
Flanking_sequencesTTATTATTTTGAGTGTAAGCTTGAGAAACATATTTCTAAAAAAAAAGACGAGCATGTTTT
Mapping_targetC34E11
Source_location225CHROMOSOME_X1180710411807104From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00007935
TranscriptC34E11.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2c.1:c.1853+158G>T
Intron_number12/13
C34E11.2g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2g.1:c.1627+158G>T
Intron_number11/12
C34E11.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2b.1:c.1685+158G>T
Intron_number11/12
C34E11.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2a.1:c.1952+158G>T
Intron_number13/15
C34E11.2f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2f.1:c.1713+158G>T
Intron_number14/15
C34E11.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2e.1:c.1995+158G>T
Intron_number14/15
C34E11.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2d.1:c.1670+158G>T
Intron_number12/14
MethodWGS_Flibotte