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WormBase Tree Display for Variation: WBVar00099607

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Name Class

WBVar00099607NamePublic_nameWBVar00099607
Other_namepas4466
F32H2.6.1:c.65+99C>A
HGVSgCHROMOSOME_I:g.8999401G>T
Sequence_detailsSMapS_parentSequenceF32H2
Flanking_sequencesggatccataggattattttgttttgaagtaccgggaaggataccagcgtcgaatttgttcaaatcttttttctttccccgtttttttggtagatctgtaaatcctggagcccaactgagttgatcttcggtcaccacgtcatcgcaggcaagaagcatgccaccgaacattttgacttctttattatcgcatctaaaagtattcgaaagatctgagaattttcaagtataatagatgtgagacctcgaattgtttcacgattgcgaacaatcaaaaattcaaaaactgaatgagtccgatacatctagctcaaaacagctagtgaaaaaaacatatctagactttgtttgtgggaacaaggaatacatacgttttgaactaaaagtctaaaacagtaccttggaatttgatcttttgatattacgatatcttcctgcttctcccaccaacgtttgggatccatgttatccgaaagctgaatttggaaattacttttgctcaacagttcaacaataaaggaatcagagtggaagctggtaaatttggaaaatcttgaaaatgaaccagacgactatcctttgtggcaaaagaagaggttga
Mapping_targetF32H2
Type_of_mutationSubstitutionGT
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004604From_analysisWGS_Pasadena_Quinlan
PersonWBPerson6900
AnalysisWGS_Pasadena_Quinlan
StatusLive
AffectsGeneWBGene00009343
TranscriptF32H2.6.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF32H2.6.1:c.65+99C>A
Intron_number2/4
MethodWGS_Pasadena_Quinlan