Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar01620964

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01620964NamePublic_nameWBVar01620964
Other_namecewivar00300685
C34E11.2g.1:c.1514-926T>C
C34E11.2e.1:c.1796-453T>C
C34E11.2b.1:c.1529-453T>C
C34E11.2f.1:c.1514-453T>C
C34E11.2c.1:c.1697-453T>C
C34E11.2a.1:c.1796-453T>C
C34E11.2d.1:c.1514-453T>C
HGVSgCHROMOSOME_X:g.11808369A>G
Sequence_detailsSMapS_parentSequenceC34E11
Flanking_sequencesTATTAGAACGTTGTACAATGGAGCACGCTTCAGACACTATTTTTCTAATTATCAGTTTTC
Mapping_targetC34E11
Source_location225CHROMOSOME_X1180830111808301From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
Strain (16)
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00007935
TranscriptC34E11.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2c.1:c.1697-453T>C
Intron_number10/13
C34E11.2g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2g.1:c.1514-926T>C
Intron_number10/12
C34E11.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2b.1:c.1529-453T>C
Intron_number9/12
C34E11.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2a.1:c.1796-453T>C
Intron_number11/15
C34E11.2f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2f.1:c.1514-453T>C
Intron_number11/15
C34E11.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2e.1:c.1796-453T>C
Intron_number11/15
C34E11.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2d.1:c.1514-453T>C
Intron_number10/14
MethodWGS_Flibotte