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WormBase Tree Display for Variation: WBVar01448128

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Name Class

WBVar01448128EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01448128
Other_nameT21C12.1e.1:c.1345-28T>A
T21C12.1m.1:c.784-28T>A
T21C12.1f.1:c.563-879T>A
T21C12.1c.2:c.1288-28T>A
T21C12.1k.1:c.1288-28T>A
T21C12.1d.1:c.1252-28T>A
T21C12.1o.1:c.59-879T>A
T21C12.1c.1:c.1288-28T>A
HGVSgCHROMOSOME_III:g.10529707T>A
Sequence_detailsSMapS_parentSequenceT21C12
Flanking_sequencesTATTTACGACTCCTCTGCAAAACCAAAAAAAGCCTTTTTTTAATCAATAAATTCCAGGCT
Mapping_targetT21C12
Type_of_mutationSubstitutionta
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00031279From_analysisWGS_Andersen
WBStrain00031284From_analysisWGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisWGS_Andersen
DB_infoDatabasedbSNP_rsrs193334385
dbSNP_ssss295510304
StatusLive
AffectsGeneWBGene00006784
TranscriptT21C12.1k.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1k.1:c.1288-28T>A
Intron_number10/11
T21C12.1m.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1m.1:c.784-28T>A
Intron_number6/8
T21C12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1c.1:c.1288-28T>A
Intron_number11/18
T21C12.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1e.1:c.1345-28T>A
Intron_number12/19
T21C12.1c.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1c.2:c.1288-28T>A
Intron_number11/14
T21C12.1o.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1o.1:c.59-879T>A
Intron_number1/5
T21C12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1d.1:c.1252-28T>A
Intron_number10/17
T21C12.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1f.1:c.563-879T>A
Intron_number6/11
ReferenceWBPaper00040707
MethodWGS_Andersen