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WormBase Tree Display for Variation: WBVar00098605

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Name Class

WBVar00098605NamePublic_nameWBVar00098605
Other_namepas3464
T13B5.1.1:c.519+27A>T
HGVSgCHROMOSOME_II:g.1093368A>T
Sequence_detailsSMapS_parentSequenceT13B5
Flanking_sequencesaattttcctgatggaggtcacagttggtcagtacctgcaaaaaggtgctatggaaatgtggctcatgtgcccacttttccgtggtgtcggaatcggtaatgtcgtgatcgccttcatgtgcatcgcctacttctgtgtaattgtcgcctgggccatgttctacatgattagctcaattgcctgggtgttcccgtgggagacttgcaacaattattggaatgatgccacgtgtgtcactggaaaggaaaactttaccgagttggcgaggattaaggtgaattcagattttgattttttgattgaaactaaaatatttggttgcaaattgactttaactaattaaaaatcacgtgttctagctaataatgtcaaaacaaaaattttatgccccaccggggatcgaaccctggtgtgttgcctaccatccatccctcttacctactgagccattagtacacattttaaaattttcgaaaaaaaatgtctgggatgttagtttttcatggtgattttgaattttcaaatatttttttgcgaaaaccaaatttgaagagtgtattttactggaatttctgagtttatacatctaacactcagcaa
Mapping_targetT13B5
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004604From_analysisWGS_Pasadena_Quinlan
PersonWBPerson6900
AnalysisWGS_Pasadena_Quinlan
StatusLive
AffectsGeneWBGene00004902
TranscriptT13B5.1.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT13B5.1.1:c.519+27A>T
Intron_number4/10
MethodWGS_Pasadena_Quinlan