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WormBase Tree Display for Variation: WBVar00269660

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Name Class

WBVar00269660NamePublic_nameWBVar00269660
Other_nameuCE3-804
haw142398
cewivar00195788
H06I04.6b.1:c.195T>C
H06I04.6b.2:c.195T>C
CE44121:p.Gly65=
H06I04.6a.1:c.-322T>C
H06I04.6a.3:c.-220T>C
H06I04.6b.3:c.195T>C
HGVSgCHROMOSOME_III:g.3064128A>G
Sequence_detailsSMapS_parentSequenceH06I04
Flanking_sequencesTCCATCCTCCACCGCTATTTGATCCCCGATTCGTGTTGGCTCCCAAGTTGGTACCCCTTGAGTAATCATTTCTTCCAGCTCCACTAGTTTTCGAGCCACCCCGAGCCAACCACCTCCAGAAGATGTTCGTGCTCCCGACGATCCTCGGCTTCCAAATCCACCGCCACTACTTCCACGGGATCCACCACCGCCACGTGAGC
Mapping_targetH06I04
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (16)
PersonWBPerson4037
AnalysisSNP_Swan
WGS_Yanai
Million_mutation_project_reanalysis
HistoryAcquires_mergeWBVar00562263
StatusLive
AffectsGeneWBGene00019170
TranscriptH06I04.6b.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScH06I04.6b.2:c.195T>C
HGVSpCE44121:p.Gly65=
cDNA_position216
CDS_position195
Protein_position65
Exon_number2/7
Codon_changeggT/ggC
Amino_acid_changeG
H06I04.6b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScH06I04.6b.1:c.195T>C
HGVSpCE44121:p.Gly65=
cDNA_position214
CDS_position195
Protein_position65
Exon_number2/8
Codon_changeggT/ggC
Amino_acid_changeG
H06I04.6a.3VEP_consequence5_prime_UTR_variant
VEP_impactMODIFIER
HGVScH06I04.6a.3:c.-220T>C
cDNA_position216
Exon_number1/7
H06I04.6b.3VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScH06I04.6b.3:c.195T>C
HGVSpCE44121:p.Gly65=
cDNA_position214
CDS_position195
Protein_position65
Exon_number2/8
Codon_changeggT/ggC
Amino_acid_changeG
H06I04.6a.1VEP_consequence5_prime_UTR_variant
VEP_impactMODIFIER
HGVScH06I04.6a.1:c.-322T>C
cDNA_position216
Exon_number1/8
ReferenceWBPaper00038208
WBPaper00005369
MethodSNP_Swan