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WormBase Tree Display for Variation: WBVar00067605

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Name Class

WBVar00067605NamePublic_nameWBVar00067605
Other_namepas25118
cewivar00061767
F13D2.1b.1:c.3646-22T>G
F13D2.1a.1:c.3580-22T>G
HGVSgCHROMOSOME_X:g.11166269A>C
Sequence_detailsSMapS_parentSequenceC05C9
Flanking_sequencescatctcaccgttacctgaaaatcattaatgttgttgtaacgtttcgtactgcgtgtttacttctagaagatcattatatgcaatttcaacggatcttctgcttttttcgaataaagatcttgatgcaacaagtgttgttaacgggcttccatacgatccatcactactctgttgttcggatatccagtcagcaagtctgtcccaatctacttcagttccttctgcatatgcagtcactattgccgctagagcaaagctgttgaccataacttgacagctctgcaacgtactgagttcgaatgtttcaactattttcaaaacttagctctctttttctgttttcagcagaacttaagaatataaaggttttgagtattacttgaatttatttttaaaatttctgtgaaaaaactaaatttaatatctaaacatacgttggattccatctataaaaaatgttcatcaaacaaattcattggcaacatatctagaaggcttttgagttttgttttcccccgaaaaagttcaactcttcattgtcaggccgcttgtttttatcatcgcgtattttatgccaatagtgaattatgtctgtggcca
Mapping_targetC05C9
Type_of_mutationSubstitutionAC
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (16)
PersonWBPerson6900
AnalysisWGS_Pasadena_Quinlan
Million_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00008735
TranscriptF13D2.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF13D2.1b.1:c.3646-22T>G
Intron_number29/38
F13D2.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF13D2.1a.1:c.3580-22T>G
Intron_number28/37
MethodWGS_Pasadena_Quinlan