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WormBase Tree Display for Variation: WBVar00144555

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Name Class

WBVar00144555NamePublic_namee2091
Other_nameC38D4.6b.2:c.764+101A>G
C38D4.6a.2:c.770+101A>G
C38D4.6a.1:c.770+101A>G
C38D4.6b.1:c.764+101A>G
C38D4.6c.1:c.626+101A>G
HGVSgCHROMOSOME_III:g.4806599T>C
Sequence_detailsSMapS_parentSequenceC38D4
Flanking_sequencescatacaccgcatcacctttaccgcctttcactctgtgccaaatcaagaaaacttgatatt
Mapping_targetC38D4
Type_of_mutationSubstitutiontcPaper_evidenceWBPaper00004312
Curator_confirmedWBPerson51134
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004520
WBStrain00007179
WBStrain00007180
WBStrain00007181
WBStrain00007183
WBStrain00007184
LaboratoryCB
StatusLive
AffectsGeneWBGene00003912
TranscriptC38D4.6b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC38D4.6b.1:c.764+101A>G
Intron_number7/8
C38D4.6a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC38D4.6a.1:c.770+101A>G
Intron_number6/7
C38D4.6b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC38D4.6b.2:c.764+101A>G
Intron_number6/7
C38D4.6c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC38D4.6c.1:c.626+101A>G
Intron_number4/5
C38D4.6a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC38D4.6a.2:c.770+101A>G
Intron_number7/8
Interactor (12)
GeneticsInterpolated_map_positionIII-2.4658
Mapping_dataIn_2_point4229
6036
In_multi_point1482
1483
2081
2083
2085
2086
DescriptionPhenotype (8)
ReferenceWBPaper00003428
WBPaper00004312
WBPaper00010528
WBPaper00022899
WBPaper00016871
WBPaper00014489
WBPaper00014562
WBPaper00004853
WBPaper00004616
WBPaper00011184
WBPaper00015464
WBPaper00022849
WBPaper00015009
WBPaper00024228
WBPaper00014356
WBPaper00014692
WBPaper00014693
WBPaper00013910
WBPaper00015661
WBPaper00021748
WBPaper00018407
RemarkCurated Sequence_details based on WBPaper00004312Paper_evidenceWBPaper00004312
Curator_confirmedWBPerson51134
MethodSubstitution_allele