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WormBase Tree Display for Variation: WBVar00023726

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Name Class

WBVar00023726NamePublic_nameWBVar00023726
Other_namepas16342
Y39G10AR.3a.1:c.654+491A>G
Y39G10AR.3b.1:c.540+491A>G
HGVSgCHROMOSOME_I:g.2360829A>G
Sequence_detailsSMapS_parentSequenceY39G10AR
Flanking_sequencestactatgtggccgaggaattgagaaaactcggtcaccagttttttgcgtccacctggaatattttgaggtgaccaaactactaaatcaatttttcacctgtttttttttgtttttttttcgtattttggccacagaattttaattaacatttcgcaatgaattacttttaaacgactggtcgagaaaaaaaattcaagaaaatcaaaaaagtttaataaaaaacgattgtctaccgcaaattttgtaattttacaaaaatcgataattttttatctttgacgaaactgaatattttagacaaagttattaagataacacaaaaatctgagaatgcgtattacacaacatatttgacgagcaaaatatctcgtaccgaaaactacagtaattctttaaatgactacagtaagtagtcaaaaagtcccatttcgttttgatcttcgaaaaatgcgggagttgagacgcagacatctcatctgatttcgcatggttaagagcgtgctgaagtcacaacttttctggaaaaatattcccgcattttttgtagatcaaattgtaatgagacagcctgacaccacgtgtaacgcttgtgtcgattt
Mapping_targetY39G10AR
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004604From_analysisWGS_Pasadena_Quinlan
PersonWBPerson6900
AnalysisWGS_Pasadena_Quinlan
StatusLive
AffectsGeneWBGene00021461
TranscriptY39G10AR.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY39G10AR.3a.1:c.654+491A>G
Intron_number5/20
Y39G10AR.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY39G10AR.3b.1:c.540+491A>G
Intron_number4/18
MethodWGS_Pasadena_Quinlan