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WormBase Tree Display for Variation: WBVar02140034

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Name Class

WBVar02140034EvidencePaper_evidenceWBPaper00045317
NamePublic_nameh5872
Other_nameF31B12.1i.1:c.4803+288C>T
F31B12.1g.1:c.4653+288C>T
F31B12.1l.1:c.4662+288C>T
F31B12.1j.1:c.4632+288C>T
F31B12.1d.1:c.4824+288C>T
F31B12.1k.1:c.4833+288C>T
F31B12.1h.1:c.4683+288C>T
HGVSgCHROMOSOME_X:g.10816710G>A
Sequence_detailsSMapS_parentSequenceF31B12
Flanking_sequencesAAGAAATTGTGAAAAACGGAGAGTGTCGAGTACAATGTTTTTCAGCATTCTGATTTGGCGACGGCTTAGGAACGCCGAAG
Mapping_targetCHROMOSOME_X
Source_location200CHROMOSOME_X1081663710816637
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023696
LaboratoryKR
AnalysisWGS_Rose
StatusLive
AffectsGeneWBGene00004036
TranscriptF31B12.1j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1j.1:c.4632+288C>T
Intron_number32/63
F31B12.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1g.1:c.4653+288C>T
Intron_number32/63
F31B12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1d.1:c.4824+288C>T
Intron_number33/64
F31B12.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1h.1:c.4683+288C>T
Intron_number32/63
F31B12.1l.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1l.1:c.4662+288C>T
Intron_number32/63
F31B12.1i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1i.1:c.4803+288C>T
Intron_number33/64
F31B12.1k.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1k.1:c.4833+288C>T
Intron_number33/64
ReferenceWBPaper00040589
WBPaper00000975
WBPaper00003985
WBPaper00000699
WBPaper00045317
MethodWGS_Rose