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: WBVar01722167

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01722167NamePublic_nameWBVar01722167
Other_namecewivar00420426
H14E04.2a.1:c.1497+225T>C
H14E04.2d.1:c.1131+225T>C
H14E04.2c.1:c.1518+225T>C
H14E04.2b.1:c.1506+225T>C
HGVSgCHROMOSOME_III:g.2383032T>C
Sequence_detailsSMapS_parentSequenceH14E04
Flanking_sequencesGGTCATACGACAAAATGCACAGTTTTTCAAATTTTGGTTTTTTACGGGCTACAAAAATGT
Mapping_targetH14E04
Source_location225CHROMOSOME_III23830222383022From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00019199
TranscriptH14E04.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2a.1:c.1497+225T>C
Intron_number9/11
H14E04.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2c.1:c.1518+225T>C
Intron_number10/12
H14E04.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2b.1:c.1506+225T>C
Intron_number9/11
H14E04.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2d.1:c.1131+225T>C
Intron_number6/8
MethodWGS_Flibotte