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: WBVar01396127

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01396127EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01396127
Other_namecewivar00673970
H14E04.2d.1:c.390-437del
H14E04.2a.1:c.756-437del
H14E04.2c.1:c.777-437del
H14E04.2b.1:c.765-437del
HGVSgCHROMOSOME_III:g.2380328del
Sequence_detailsSMapS_parentSequenceH14E04
Flanking_sequencesTTTTCAGAATTTTACAGTATTCTAGCAGTGTTAAAACAGAGGAAAAATTGAAAAAAATGTTGAATTTCAAAAAAAAAAAAAAATTTTTTTTGACAACAAA
Mapping_targetH14E04
Type_of_mutationDeletionAPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (22)
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539115311
StatusLive
AffectsGeneWBGene00019199
TranscriptH14E04.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2a.1:c.756-437del
Intron_number6/11
H14E04.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2c.1:c.777-437del
Intron_number7/12
H14E04.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2b.1:c.765-437del
Intron_number6/11
H14E04.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2d.1:c.390-437del
Intron_number3/8
ReferenceWBPaper00037807
MethodWGS_De_Bono