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WormBase Tree Display for Variation: WBVar00038286

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Name Class

WBVar00038286NamePublic_nameWBVar00038286
Other_namepas19254
cewivar00080053
F56D12.1d.1:c.951C>T
CE33403:p.Val457=
F56D12.1a.1:c.1371C>T
CE29047:p.Val457=
F56D12.1b.1:c.1371C>T
CE40074:p.Val317=
F56D12.1a.2:c.1371C>T
HGVSgCHROMOSOME_II:g.1307274G>A
Sequence_detailsSMapS_parentSequenceF56D12
Flanking_sequencesaagatttcgaattttccgggaataattttaaatcgacttttggcagttttcttgtgcctaaaatgttgaatttcagcatttttgaacataacaaacccgaaaattcgagtttttcttctttccgctgggtttttagataaaatttttgagtccctgaaaacctgtgcaaaaacttgtattttttgtagttgccaacctataaaggaactccttatcctgcgaaaaaacggcgccagtcagcccataaggtgtcgcgtctttcacagtcgcgagcacctcatcaaccttcgaatcctcgtaaccagtaccgtcaccaccggtccgaacatttcctcagtgagaagcttgctcttcggatccgtcacagtgatcagggtcggctcgatgaagtatcccgttttgtcgtcacattttccgccgagcaccacatttgctccgtcggctccggttttcgcaaagtcaatgtaggccttgagcctggcaaacgccttatcatcgatcacagccgacagaaagacggatccatcgcgaacctgtaaactacaaactacacaaaaatcggcaagccaaacagtggcctacatctccaagcttgatctc
Mapping_targetF56D12
Type_of_mutationSubstitutionGA
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.1371C>T
HGVSpCE33403:p.Val457=
cDNA_position1373
CDS_position1371
Protein_position457
Exon_number7/8
Codon_changegtC/gtT
Amino_acid_changeV
F56D12.1a.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1a.2:c.1371C>T
HGVSpCE29047:p.Val457=
cDNA_position1470
CDS_position1371
Protein_position457
Exon_number8/10
Codon_changegtC/gtT
Amino_acid_changeV
F56D12.1a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1a.1:c.1371C>T
HGVSpCE29047:p.Val457=
cDNA_position1374
CDS_position1371
Protein_position457
Exon_number7/9
Codon_changegtC/gtT
Amino_acid_changeV
F56D12.1d.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF56D12.1d.1:c.951C>T
HGVSpCE40074:p.Val317=
cDNA_position951
CDS_position951
Protein_position317
Exon_number3/4
Codon_changegtC/gtT
Amino_acid_changeV
MethodWGS_Pasadena_Quinlan