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: WBVar01548518

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01548518NamePublic_nameWBVar01548518
Other_namecewivar00124290
H14E04.2c.1:c.1518+202C>T
H14E04.2d.1:c.1131+202C>T
H14E04.2b.1:c.1506+202C>T
H14E04.2a.1:c.1497+202C>T
HGVSgCHROMOSOME_III:g.2383009C>T
Sequence_detailsSMapS_parentSequenceH14E04
Flanking_sequencesCCGAAAGTTTGCAAACACCGTAGGGTCATAGACAAAATGCACAGTTTTTCAATATTTTGG
Mapping_targetH14E04
Source_location225CHROMOSOME_III23829992382999From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004599From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00019199
TranscriptH14E04.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2a.1:c.1497+202C>T
Intron_number9/11
H14E04.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2c.1:c.1518+202C>T
Intron_number10/12
H14E04.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2b.1:c.1506+202C>T
Intron_number9/11
H14E04.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2d.1:c.1131+202C>T
Intron_number6/8
MethodWGS_Flibotte