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: WBVar01466566

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01466566EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01466566
Other_nameY113G7A.6a.1:c.1073-314A>T
Y113G7A.6d.1:c.1037-314A>T
Y113G7A.6c.1:c.962-314A>T
Y113G7A.6b.1:c.914-314A>T
HGVSgCHROMOSOME_V:g.20054498T>A
Sequence_detailsSMapS_parentSequenceY113G7A
Flanking_sequencesAACTCGAGATTTTCAGGCCGTTTCAAGCCGATTTCAGGCCAAAACTGAAAATTTTTCGAAAAATAGTTAA
Mapping_targetY113G7A
Type_of_mutationSubstitutionta
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (103)
LaboratoryQX
PersonWBPerson1730
AnalysisWGS_Andersen
DB_infoDatabasedbSNP_rsrs193352067
dbSNP_ssss295527986
StatusLive
AffectsGeneWBGene00006652
TranscriptY113G7A.6c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY113G7A.6c.1:c.962-314A>T
Intron_number7/7
Y113G7A.6a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY113G7A.6a.1:c.1073-314A>T
Intron_number9/10
Y113G7A.6b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY113G7A.6b.1:c.914-314A>T
Intron_number7/8
Y113G7A.6d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY113G7A.6d.1:c.1037-314A>T
Intron_number8/9
ReferenceWBPaper00040707
MethodWGS_Andersen