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WormBase Tree Display for Variation: WBVar01660998

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Name Class

WBVar01660998NamePublic_nameWBVar01660998
Other_namecewivar00348965
CE50538:p.Asn62=
C49C3.4b.1:c.375T>C
CE19743:p.Asn709=
CE48513:p.Asn125=
C49C3.4c.1:c.186T>C
C49C3.4a.1:c.2127T>C
HGVSgCHROMOSOME_IV:g.17324193T>C
Sequence_detailsSMapS_parentSequenceC49C3
Flanking_sequencesGGAAGGGTCCATAATCATCCTCCTTGTAAACGTTTGCCTAAGAATGATGATGACCTTATT
Mapping_targetC49C3
Source_location225CHROMOSOME_IV1732415617324156From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006631From_analysisMillion_mutation_project_reanalysis
WBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00022899From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00008194
TranscriptC49C3.4c.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC49C3.4c.1:c.186T>C
HGVSpCE50538:p.Asn62=
cDNA_position186
CDS_position186
Protein_position62
Exon_number3/15
Codon_changeaaT/aaC
Amino_acid_changeN
C49C3.4b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC49C3.4b.1:c.375T>C
HGVSpCE48513:p.Asn125=
cDNA_position375
CDS_position375
Protein_position125
Exon_number4/16
Codon_changeaaT/aaC
Amino_acid_changeN
C49C3.4a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC49C3.4a.1:c.2127T>C
HGVSpCE19743:p.Asn709=
cDNA_position2130
CDS_position2127
Protein_position709
Exon_number11/24
Codon_changeaaT/aaC
Amino_acid_changeN
MethodWGS_Flibotte