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WormBase Tree Display for Variation: WBVar00049781

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Name Class

WBVar00049781NamePublic_nameWBVar00049781
Other_namepas21553
cewivar00058273
F08C6.2a.1:c.20+830A>T
F08C6.7.1:c.213+18T>A
HGVSgCHROMOSOME_X:g.7573206A>T
Sequence_detailsSMapS_parentSequenceF08C6
Flanking_sequencestaaaaacaataaaacaaacctgttgatcactgccatccaaagcaccgccactcgattttgttggagtttgagcacttgaacttccgacctacaataatttacttgatgcttttaaaatcaaattaggatggcgctgttttaaagtatttaagcgttttcagacactattcagataattcaacattttttcacttgtatccaagggttgaaaaatgtcagtatgaatccaatcttaaaaacatttaaaaaaatttgccttaaaacctatcaaacatttcaatctctgaaattcttttttttaattttaccaaactcacatatgcttcaactgttggggcaacaactttcatgatctctttgggcttttccttatttccattttctgacgattctccattgatgccgaaggtttctagaccatgaaccatctggaaggtatttttttaatcatttcgcaatacagacacccccgcgtttttctccggtttttccgtcatctctcggtttctctaactcacttcattgttcttcacggacatcttggcaagatcacaggcattcatcaactcttcgaagtcatctctttcctttcttgcctaa
Mapping_targetF08C6
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (26)
PersonWBPerson6900
AnalysisWGS_Pasadena_Quinlan
Million_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006827
WBGene00017241
TranscriptF08C6.7.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF08C6.7.1:c.213+18T>A
Intron_number4/8
F08C6.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF08C6.2a.1:c.20+830A>T
Intron_number1/6
MethodWGS_Pasadena_Quinlan