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WormBase Tree Display for Variation: WBVar00273984

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Name Class

WBVar00273984EvidencePaper_evidenceWBPaper00005369
NamePublic_nameWBVar00273984
Other_name (11)
HGVSgCHROMOSOME_X:g.1552427G>C
Sequence_detailsSMapS_parentSequenceK06A9
Flanking_sequencesTCCACGACTTCGGGAGATATGACATCGCAAGGTTCAACTCAGATACCAGGTAGTACAGGATCCACAGTGACTCAACCGTCTACAGGTAGTGGTTCCACAACACATCAGGAGAAATCACATCCCAAGGTTCCACTCAAACACCAAGATCTTCATTGTCAACTTCTCCTGCTATTTCTACATCAACGCAACAATCAGTGTCC
Mapping_targetK06A9
Type_of_mutationSubstitutionGC
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisSNP_Swan
AnalysisSNP_Swan
StatusLive
AffectsGeneWBGene00019435
TranscriptK06A9.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK06A9.1d.1:c.3532+1087G>C
Intron_number7/12
K06A9.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK06A9.1c.1:c.1894+1087G>C
Intron_number8/14
K06A9.1b.1 (12)
K06A9.1g.1 (12)
K06A9.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK06A9.1e.1:c.4279+340G>C
Intron_number7/12
K06A9.1f.1 (12)
K06A9.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK06A9.1a.1:c.2770+1849G>C
Intron_number8/14
ReferenceWBPaper00005369
MethodSNP_Swan