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WormBase Tree Display for Variation: WBVar00099931

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Name Class

WBVar00099931NamePublic_nameWBVar00099931
Other_namepas4790
R04F11.4c.1:c.176+46T>G
R04F11.4d.1:c.110+46T>G
HGVSgCHROMOSOME_V:g.12335777A>C
Sequence_detailsSMapS_parentSequenceR04F11
Flanking_sequencesagtcactcatgtgaaactaaattgatgatcaacataatatctaaaaataagttattattatagaatcaaaacaaaaatatcgataaaatgggtataaaaccgagaaaaagttccgccgacatataaatgtccggattaaattgtcaaaactctctcaaagttgagagagagagagagagacacgccgcggctcccgacccaaaaaattgttttctggttgttcgaagaaacggacacgaagtagtaaactgattattgaataagcgagacatcagttgacaacgaagagtcgtcagaaaaggacaagaacccgaaaaaaccgttggtaaaatgaaagaaacttactcatcaagatgtgttgacctagctgtgtgcatcgaattccggttcgaaaagtccgattcgcggtagctttgtggtagagatctgaaatttttttaaaatgaacttgaatgtttgaatttttggtttaaaagttgtattggcattaccttaaatgcactttcacatgctatgtcacatcattttttggttctgtgtcattctcgacatgctttttagcttttgaaaatttaaactaagtatttaacatttttgggg
Mapping_targetR04F11
Type_of_mutationSubstitutionAC
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004604From_analysisWGS_Pasadena_Quinlan
PersonWBPerson6900
AnalysisWGS_Pasadena_Quinlan
StatusLive
AffectsGeneWBGene00006668
TranscriptR04F11.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR04F11.4d.1:c.110+46T>G
Intron_number2/12
R04F11.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR04F11.4c.1:c.176+46T>G
Intron_number4/15
MethodWGS_Pasadena_Quinlan