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WormBase Tree Display for Variation: WBVar01858753

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Name Class

WBVar01858753NamePublic_nameWBVar01858753
Other_namecewivar00572230
CE05332:p.Ser655=
C29E6.1c.1:c.1965C>T
C29E6.1b.1:c.1845C>T
CE37323:p.Ser615=
CE40548:p.Ser774=
C29E6.1a.1:c.2322C>T
HGVSgCHROMOSOME_IV:g.11890727C>T
Sequence_detailsSMapS_parentSequenceC29E6
Flanking_sequencesAAATCCGTCGAAATCTAAAAATTTCACAAGGTTGTTGGTTGGTTCAAATTTAGTTTATTT
Mapping_targetC29E6
Source_location225CHROMOSOME_IV1189070411890704From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00002827
TranscriptC29E6.1b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC29E6.1b.1:c.1845C>T
HGVSpCE37323:p.Ser615=
cDNA_position1850
CDS_position1845
Protein_position615
Exon_number9/11
Codon_changeagC/agT
Amino_acid_changeS
C29E6.1a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC29E6.1a.1:c.2322C>T
HGVSpCE40548:p.Ser774=
cDNA_position2325
CDS_position2322
Protein_position774
Exon_number10/12
Codon_changeagC/agT
Amino_acid_changeS
C29E6.1c.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC29E6.1c.1:c.1965C>T
HGVSpCE05332:p.Ser655=
cDNA_position1965
CDS_position1965
Protein_position655
Exon_number9/10
Codon_changeagC/agT
Amino_acid_changeS
MethodWGS_Flibotte