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WormBase Tree Display for Variation: WBVar01640929

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Name Class

WBVar01640929NamePublic_nameWBVar01640929
Other_namecewivar00323065
CE33588:p.Val8178=
ZK973.6c.1:c.24513T>G
CE52283:p.Val7173=
ZK973.6a.1:c.24534T>G
CE52179:p.Val8171=
ZK973.6b.1:c.21519T>G
HGVSgCHROMOSOME_I:g.4357553T>G
Sequence_detailsSMapS_parentSequenceZK973
Flanking_sequencesTTGGTGAAAAATTGGCTGCACTTGCCGCTTTCAATGCCGCTCGCAAAAATGCCGAAGACGCCCTTCTCGATATCACCCGTGAAGATGGAGGTGATGACAACAAATCACCAGACGAGCTTATTGATGATCTAGCCAAGAAGGAGGAAACTGTTGCCAAGCTTCTTGATACTGTTTCCGGAGTTAAGCCTGACGAGCTCGATGATAAGGAACGAGCTGAATACAACGACTTGCTTGCAAGACTCGCGACCGCGGCTGACGTTCTGAAAGTAAGTCAATGTTTTAAATGATCTAGATATAATTGCGTTTATGCTGTAAATTCAAGTATTCCTTAGATAACACGCTTTTTCTTGGTTTCTTAAAATCAAGTGCCTACCTTACCTAAGTGCCTAGCGACCTTAAAAATTTCACTTCCAAGGTATCAATTTTAATTACTATTATTTTCAGAACAAACGTGCCGAACTCGAACAAGCAGTCAAGGCCAAGGCCGACGAGAAATCGCTACACGACTCTGTTGACCGTATCGTATCTCGTCTTGTGCCACTTGTTCGTGAATCGGATGAGCTCCGTCACAACGCTGAAGCCGTTCCTACTCAATACGCTCCAAAGGCCGAAGAACTGAAGAAGGAGGTCGAAGCTGCGAAGGCCGTCATCGCCAACGCTCCATCGTCTGATGCTCATGTCAACAACTCGAACAAGCTGTTGCAACCGCA
Mapping_targetZK973
Source_location225CHROMOSOME_I43575544357554From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00023018From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000140
TranscriptZK973.6c.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScZK973.6c.1:c.24513T>G
HGVSpCE52179:p.Val8171=
cDNA_position24513
CDS_position24513
Protein_position8171
Exon_number26/30
Codon_changegtT/gtG
Amino_acid_changeV
ZK973.6b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScZK973.6b.1:c.21519T>G
HGVSpCE52283:p.Val7173=
cDNA_position21605
CDS_position21519
Protein_position7173
Exon_number16/20
Codon_changegtT/gtG
Amino_acid_changeV
ZK973.6a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScZK973.6a.1:c.24534T>G
HGVSpCE33588:p.Val8178=
cDNA_position24534
CDS_position24534
Protein_position8178
Exon_number26/31
Codon_changegtT/gtG
Amino_acid_changeV
MethodWGS_Flibotte