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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)
Reference (21)
RemarkCurated Sequence_details based on WBPaper00004312Paper_evidenceWBPaper00004312
Curator_confirmedWBPerson51134
MethodSubstitution_allele