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WormBase Tree Display for Variation: WBVar02139035

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Name Class

WBVar02139035EvidencePaper_evidenceWBPaper00045317
NamePublic_nameh13633
Other_nameF56B6.2h.1:c.1711+1128G>A
F56B6.2j.1:c.1705+1128G>A
F56B6.2e.1:c.211+1128G>A
F56B6.2c.1:c.511+1128G>A
F56B6.2i.1:c.1702+1128G>A
F56B6.2b.1:c.1585+1128G>A
F56B6.2a.1:c.1696+1128G>A
HGVSgCHROMOSOME_X:g.3551399G>A
Sequence_detailsSMapS_parentSequenceF56B6
Flanking_sequencesTTATCAGAGAGCCCTCGGTTTATGGAAACAGTGTGAGGTGAAGTGATGCCTAGCCGTCAACCAAAATTGTTTATGAAGCC
Mapping_targetCHROMOSOME_X
Source_location200CHROMOSOME_X35513873551387
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023740
LaboratoryKR
AnalysisWGS_Rose
StatusLive
AffectsGeneWBGene00004350
TranscriptF56B6.2j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2j.1:c.1705+1128G>A
Intron_number9/14
F56B6.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2e.1:c.211+1128G>A
Intron_number1/7
F56B6.2i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2i.1:c.1702+1128G>A
Intron_number10/16
F56B6.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2b.1:c.1585+1128G>A
Intron_number9/15
F56B6.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2a.1:c.1696+1128G>A
Intron_number10/16
F56B6.2h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2h.1:c.1711+1128G>A
Intron_number10/16
F56B6.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2c.1:c.511+1128G>A
Intron_number4/9
ReferenceWBPaper00040589
WBPaper00000975
WBPaper00003985
WBPaper00000699
WBPaper00045317
MethodWGS_Rose