Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar01593989

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01593989NamePublic_nameWBVar01593989
Other_namecewivar00254109
T20B3.2.1:c.57+13T>C
T20B3.7.2:c.208+1517A>G
T20B3.7.1:c.208+1517A>G
HGVSgCHROMOSOME_V:g.16835040A>G
Sequence_detailsSMapS_parentSequenceT20B3
Flanking_sequencesTGAAATTAATTTTAAGTAATCTGAAAATTGGCAACTTCTTACGTCCTCAACATCAGCCTG
Mapping_targetT20B3
Source_location225CHROMOSOME_V1683501816835018From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
WBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006585
WBGene00004026
TranscriptT20B3.2.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT20B3.2.1:c.57+13T>C
Intron_number2/5
T20B3.7.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT20B3.7.1:c.208+1517A>G
Intron_number3/7
T20B3.7.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT20B3.7.2:c.208+1517A>G
Intron_number2/6
MethodWGS_Flibotte