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WormBase Tree Display for Variation: WBVar01454417

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Name Class

WBVar01454417EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01454417
Other_nameZK617.1f.1:c.1747-388A>G
ZK617.1c.1:c.130-388A>G
ZK617.1g.1:c.1747-388A>G
ZK617.1h.1:c.1747-388A>G
ZK617.1b.1:c.1747-388A>G
ZK617.1i.1:c.1747-388A>G
ZK617.1d.1:c.586-388A>G
ZK617.1a.1:c.1747-388A>G
HGVSgCHROMOSOME_IV:g.11997251T>C
Sequence_detailsSMapS_parentSequenceZK617
Flanking_sequencesTATTTTAAATTTAGATAGTTCCTGAAATTTATAAATTTCAATTTTTGTTTAAATTTGGGT
Mapping_targetZK617
Type_of_mutationSubstitutiontc
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (51)
LaboratoryQX
PersonWBPerson1730
AnalysisWGS_Andersen
DB_infoDatabasedbSNP_rsrs193340074
dbSNP_ssss295515993
StatusLive
AffectsGeneWBGene00006759
TranscriptZK617.1i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK617.1i.1:c.1747-388A>G
Intron_number11/32
ZK617.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK617.1a.1:c.1747-388A>G
Intron_number12/32
ZK617.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK617.1g.1:c.1747-388A>G
Intron_number11/31
ZK617.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK617.1f.1:c.1747-388A>G
Intron_number11/30
ZK617.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK617.1d.1:c.586-388A>G
Intron_number2/21
ZK617.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK617.1c.1:c.130-388A>G
Intron_number3/25
ZK617.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK617.1h.1:c.1747-388A>G
Intron_number11/33
ZK617.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK617.1b.1:c.1747-388A>G
Intron_number11/33
ReferenceWBPaper00040707
MethodWGS_Andersen