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WormBase Tree Display for Variation: WBVar00234511

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Name Class

WBVar00234511NamePublic_nameWBVar00234511
Other_namepas46287
F59C12.1b.1:c.838+120del
F59C12.1a.1:c.838+120del
HGVSgCHROMOSOME_X:g.16598614del
Sequence_detailsSMapS_parentSequenceF59C12
Flanking_sequencesccacactgtactaaacttgattactgtcaaactgctatagctactgcttttttctctcgctcaccaaaaaagctactattcaaacgttttcagaatggcgtattggttttcgaaccggaggctatctcagcacaagatggcgatcgtctcaacgcttcgctgatcttttctctgtccggaggtatgtaaggggggcgcctgcatatcatttcatacctcatgttgcgtgccttatgcgcacgaattcaaaccaaatggggagaagatttggaagaaaacgaaacaatcgaaccaaaaaacaaaaaaaacacaatatcgacaatttcactaggaggagaaatttcgagaaggggtgaatgttttgagggagcaaatagaatacttttatgaaagtaaaacctaggctattttatatggcgttatgacgttgctcggaatagttcttcgtgaccgtctttttttttgaaatactacaaattttgaataatgggcacacgaacaatttttcaatttctcaatcatcattattttaataaaagttgttaattttgaggcaagctctgacgtaaattgaccatagttttgctcaagttgcattt
Mapping_targetF59C12
Type_of_mutationDeletionA
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004604From_analysisWGS_Pasadena_Quinlan
PersonWBPerson6900
AnalysisWGS_Pasadena_Quinlan
StatusLive
AffectsGeneWBGene00000401
TranscriptF59C12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF59C12.1a.1:c.838+120del
Intron_number7/15
F59C12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF59C12.1b.1:c.838+120del
Intron_number7/15
MethodWGS_Pasadena_Quinlan