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WormBase Tree Display for Variation: WBVar00050491

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Name Class

WBVar00050491NamePublic_nameWBVar00050491
Other_namepas21695
cewivar00058481
K09F5.6a.1:c.2397+245A>G
CE53611:p.Gly838=
K09F5.6b.1:c.2514A>G
HGVSgCHROMOSOME_X:g.7724363A>G
Sequence_detailsSMapS_parentSequenceK09F5
Flanking_sequencesggcaaccaggtcaattgctatggaaccctccaggagctacaaacggacacaataaggttattttatctatttgagttgttgtattcgagcttttctctcattatttcaattttttgcacgatgagttatttattcattcacattttcggcacacatctcattctaacatccacatccattgcagtcatcgctaaccagcacaacaaattcatctcaaaacgatgagcaatgctttaccccgacttcaacactaacaagtcacggaagtaactacactccaacacctggatctccacaaggtccaatccgatctattcccgaatcaatggagcatcttccacatcgtcaaatctttacggagttgcttccaaagaaagtcaatatgctgacaggacacttcaaaaagcaccgatcaaatctacaacagtgacgactggaaatacaatacttcgttccgtgaacggaacagatgacactgtatcaagcttttctcgtccacccactggagcacttaaccaaaatgactttgctaccagcattgtgtgaatatttgttttacatttttggtaggtcttaattcaaaagtaactagaaatgttt
Mapping_targetK09F5
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (27)
PersonWBPerson6900
AnalysisWGS_Pasadena_Quinlan
Million_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00044698
TranscriptK09F5.6b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScK09F5.6b.1:c.2514A>G
HGVSpCE53611:p.Gly838=
cDNA_position2650
CDS_position2514
Protein_position838
Exon_number13/15
Codon_changeggA/ggG
Amino_acid_changeG
K09F5.6a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK09F5.6a.1:c.2397+245A>G
Intron_number12/13
MethodWGS_Pasadena_Quinlan