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WormBase Tree Display for Variation: WBVar00038346

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Name Class

WBVar00038346NamePublic_nameWBVar00038346
Other_name (11)
HGVSgCHROMOSOME_II:g.1308844A>G
Sequence_detailsSMapS_parentSequenceF56D12
Flanking_sequencesccagcagacccaatcttatcaaaatcacattggtctgctaaatcgaaatttgtagtttgtagtctagcagacccaatttctacaaaaccaaatcggcaaatttgaggaatttcagcttaatttagcaatttttctcggaaattttcaaattttcatcacgaatttcggcttttcaaggctatttctagttttttggcacaccataagcgccggagcagtcggcaaatttcctccgatcgccgtaaaattgaacggtgcgattgcggcgacgaatccctccattccacggaactgcatcgttttttggtgattttcgtggaaatcggctcataatgctccagctccatagcgaaaaccgcgttgaatcggaagaaatcgatgagctcacaggcggcgtcaatttcagcctgaataatattctttccctggccgagcatcgtggaggcgttcagcttcattcggtactttccagcggccaaatcggcggcgcggagcaaaatttcagctcgttctctgaaaatctgacgattttatagcgaaatcccctggcgtatttgctcacttaagcggttttctctcccaggcgcctctcgcctgaag
Mapping_targetF56D12
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000034From_analysisMillion_mutation_project_reanalysis
WBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00004604From_analysisWGS_Pasadena_Quinlan
WBStrain00006625From_analysisMillion_mutation_project_reanalysis
WBStrain00023665From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
PersonWBPerson6900
AnalysisWGS_Pasadena_Quinlan
Million_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000112
TranscriptF56D12.1b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1b.1:c.579T>C
HGVSpCE33403:p.Asn193=
cDNA_position581
CDS_position579
Protein_position193
Exon_number5/8
Codon_changeaaT/aaC
Amino_acid_changeN
F56D12.1a.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1a.2:c.579T>C
HGVSpCE29047:p.Asn193=
cDNA_position678
CDS_position579
Protein_position193
Exon_number6/10
Codon_changeaaT/aaC
Amino_acid_changeN
F56D12.1a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1a.1:c.579T>C
HGVSpCE29047:p.Asn193=
cDNA_position582
CDS_position579
Protein_position193
Exon_number5/9
Codon_changeaaT/aaC
Amino_acid_changeN
F56D12.1d.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1d.1:c.159T>C
HGVSpCE40074:p.Asn53=
cDNA_position159
CDS_position159
Protein_position53
Exon_number1/4
Codon_changeaaT/aaC
Amino_acid_changeN
F56D12.1c.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1c.1:c.579T>C
HGVSpCE37118:p.Asn193=
cDNA_position579
CDS_position579
Protein_position193
Exon_number4/6
Codon_changeaaT/aaC
Amino_acid_changeN
MethodWGS_Pasadena_Quinlan