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WormBase Tree Display for Variation: WBVar00050481

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Name Class

WBVar00050481NamePublic_nameWBVar00050481
Other_namepas21693
cewivar00058479
K09F5.6b.1:c.1356+12C>G
K09F5.6a.1:c.1356+12C>G
HGVSgCHROMOSOME_X:g.7722507C>G
Sequence_detailsSMapS_parentSequenceK09F5
Flanking_sequencestcgacgacgctcctacacaagagtcgatggaaacaagttgtgctgtgatggttatttgccacatatggatgccattgcacttttagtcattgttgctggagcgattggtcctaccatctacgctctgttgattctttatcagcatgaacaaaaagcattaatactgacttgcatcataattgacgtcgtctacatgttttcatggattctgatgtggcttggaatgaccttaaaaagagattgggattttaatgttacgcataaagttcatcagttctatggattgaatgtaagtttgaaaataaattgatagtgtcaagcagaattattttcagaaaggaatggcaattggaccaattcgtggaaatgaaaatccatctcaactgaaaaactctattcttgttgttcatcgtgatactgtaagtacatattagttcttaaaagtgaaacaagcattatttttttaaagatgtttgtgaccgatgaccaaacagcaaaacaatcgcttcttcgagcaattcacagtggaaagtttgaaatgataagtccacccgatgatgtgtactggaggcaaggtcaacaaagtcctgcaactcgggc
Mapping_targetK09F5
Type_of_mutationSubstitutionCG
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (27)
PersonWBPerson6900
AnalysisWGS_Pasadena_Quinlan
Million_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00044698
TranscriptK09F5.6b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK09F5.6b.1:c.1356+12C>G
Intron_number7/14
K09F5.6a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK09F5.6a.1:c.1356+12C>G
Intron_number7/13
MethodWGS_Pasadena_Quinlan