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WormBase Tree Display for Variation: WBVar00223670

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Name Class

WBVar00223670NamePublic_nameWBVar00223670
Other_name (16)
HGVSgCHROMOSOME_II:g.5219040C>T
Sequence_detailsSMapS_parentSequenceC34F11
Flanking_sequencesttgaatgtaaatttttttcaatgttgcatattccttgagatagccctgcaagacctgaatgtagccctattataacttaaacttttgctttaattttttataaataaaaatttgccgaataaaatacactaaattttgaaaggaacactgtcaccagagtactggctttacataaaaattcaatgaaatgaaacctatgtttataaaattaaaaaaaaaaacatacctatcatcatcatctgaaaatactcttgcatcggattcggagccaattgttgattcttcgagatgtcgtcggtgcctggaatttaagaaaacttagaattcgatgctttttcaaattttcataagattttgttttttgaacctattaccctttacttgatcacatcatttttcgccatcatttacctaccgatcaaataaaacgatgcatctgcactaagttcagaggttaaggatagatgtgacgtcctatgtagaaatccaataagatgtcttctcggcgaagcatccggtgcaacatctttccttccttgataagtacttgttgtatttgatccgccgtaccttcgcattctgcgcttctgtgctcgatcc
Mapping_targetC34F11
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (69)
LaboratoryQX
AX
PersonWBPerson6900
WBPerson1730
AnalysisWGS_Pasadena_Quinlan
WGS_De_Bono
Million_mutation_project_reanalysis
WGS_Andersen
HistoryAcquires_mergeWBVar01239970
WBVar01437734
StatusLive
AffectsGeneWBGene00001101
TranscriptC34F11.9f.1VEP_consequencesplice_region_variant,synonymous_variant
VEP_impactLOW
HGVScC34F11.9f.1:c.96G>A
HGVSpCE50486:p.Gly32=
cDNA_position96
CDS_position96
Protein_position32
Exon_number2/9
Codon_changeggG/ggA
Amino_acid_changeG
C34F11.9e.1VEP_consequencesplice_region_variant,synonymous_variant
VEP_impactLOW
HGVScC34F11.9e.1:c.1521G>A
HGVSpCE50427:p.Gly507=
cDNA_position1521
CDS_position1521
Protein_position507
Exon_number2/10
Codon_changeggG/ggA
Amino_acid_changeG
C34F11.9c.1VEP_consequencesplice_region_variant,synonymous_variant
VEP_impactLOW
HGVScC34F11.9c.1:c.684G>A
HGVSpCE43370:p.Gly228=
cDNA_position692
CDS_position684
Protein_position228
Exon_number7/16
Codon_changeggG/ggA
Amino_acid_changeG
C34F11.9b.1VEP_consequencesplice_region_variant,synonymous_variant
VEP_impactLOW
HGVScC34F11.9b.1:c.1521G>A
HGVSpCE48076:p.Gly507=
cDNA_position1558
CDS_position1521
Protein_position507
Exon_number3/10
Codon_changeggG/ggA
Amino_acid_changeG
C34F11.9a.1VEP_consequencesplice_region_variant,synonymous_variant
VEP_impactLOW
HGVScC34F11.9a.1:c.684G>A
HGVSpCE43333:p.Gly228=
cDNA_position693
CDS_position684
Protein_position228
Exon_number7/14
Codon_changeggG/ggA
Amino_acid_changeG
C34F11.9d.1VEP_consequencesplice_region_variant,synonymous_variant
VEP_impactLOW
HGVScC34F11.9d.1:c.96G>A
HGVSpCE50407:p.Gly32=
cDNA_position96
CDS_position96
Protein_position32
Exon_number2/10
Codon_changeggG/ggA
Amino_acid_changeG
C34F11.9b.2VEP_consequencesplice_region_variant,synonymous_variant
VEP_impactLOW
HGVScC34F11.9b.2:c.1521G>A
HGVSpCE48076:p.Gly507=
cDNA_position2254
CDS_position1521
Protein_position507
Exon_number8/15
Codon_changeggG/ggA
Amino_acid_changeG
C34F11.9a.2VEP_consequencesplice_region_variant,synonymous_variant
VEP_impactLOW
HGVScC34F11.9a.2:c.684G>A
HGVSpCE43333:p.Gly228=
cDNA_position700
CDS_position684
Protein_position228
Exon_number7/15
Codon_changeggG/ggA
Amino_acid_changeG
ReferenceWBPaper00040707
WBPaper00037807
MethodWGS_Pasadena_Quinlan