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WormBase Tree Display for Variation: WBVar01267983

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Name Class

WBVar01267983EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01267983
Other_namecewivar00023802
T21C12.1e.1:c.*673+43A>G
T21C12.1o.1:c.732+43A>G
T21C12.1f.1:c.1236+43A>G
T21C12.1c.1:c.*673+43A>G
T21C12.1i.1:c.363+43A>G
T21C12.9:n.101T>C
T21C12.1h.1:c.684+43A>G
T21C12.1d.1:c.*673+43A>G
HGVSgCHROMOSOME_III:g.10532382A>G
Sequence_detailsSMapS_parentSequenceT21C12
Flanking_sequencesCTCTTGTTGTAAGTGACCGAGATTTTGCATTTTGACAAACTGACACACTTTTTTTTTCTAAAACTACATTATTTCCTTTGGAGTTTTATAAATATTGAAA
Mapping_targetT21C12
Type_of_mutationSubstitutionaGPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (14)
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539103129
StatusLive
AffectsGeneWBGene00198818
WBGene00006784
TranscriptT21C12.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1h.1:c.684+43A>G
Intron_number5/6
T21C12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1c.1:c.*673+43A>G
Intron_number18/18
T21C12.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1e.1:c.*673+43A>G
Intron_number19/19
T21C12.9VEP_consequencenon_coding_transcript_exon_variant
VEP_impactMODIFIER
HGVScT21C12.9:n.101T>C
cDNA_position101
Exon_number1/1
T21C12.1o.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1o.1:c.732+43A>G
Intron_number5/5
T21C12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1d.1:c.*673+43A>G
Intron_number17/17
T21C12.1i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1i.1:c.363+43A>G
Intron_number2/2
T21C12.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1f.1:c.1236+43A>G
Intron_number10/11
ReferenceWBPaper00037807
MethodWGS_De_Bono