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WormBase Tree Display for Variation: WBVar00220494

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Name Class

WBVar00220494EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar00220494
Other_namepas32270
cewivar00088267
CE38746:p.Gly88=
Y49F6B.12.1:c.264T>C
HGVSgCHROMOSOME_II:g.3472153A>G
Sequence_detailsSMapS_parentSequenceY49F6B
Flanking_sequencesgagaaaaaatattgagctttgggaaattattctgcaagttgttactgctggaacggtgacctgtggctgttttgcattggctttagtgtcactaaattgatctgacataagttggttttacaatcgttcgcctattgaaatatatagaacaccgaactctatagaagttaatgctatattatttttatgtcaaaaatttattattatatttcacagaaattattagatttccgcctgctgcataccattaccacgttccattcctgatttcccattttccttctcttccggcattccttgccatttgaattcattccattcattccgctcatcccattattcttacccattccagcttgtccttcctgaccagtcggcattcctcgtccactctcacccatctggccttcctggcttctaggcattccttgtcctccatccataccttcccggtgcattccatcttgacctcccatttttccttgttgaaccatatcagtctcagcacttagtgcgccagaaataacgagtatagccaaaagtgcacagaagaaggatgacatgattgaaagttgatagccttggtgatgcaggcctggg
Mapping_targetY49F6B
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (30)
LaboratoryQX
PersonWBPerson6900
WBPerson1730
AnalysisWGS_Pasadena_Quinlan
Million_mutation_project_reanalysis
WGS_Andersen
HistoryAcquires_mergeWBVar01436987
StatusLive
AffectsGeneWBGene00044376
TranscriptY49F6B.12.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScY49F6B.12.1:c.264T>C
HGVSpCE38746:p.Gly88=
cDNA_position264
CDS_position264
Protein_position88
Exon_number1/1
Codon_changeggT/ggC
Amino_acid_changeG
ReferenceWBPaper00040707
MethodWGS_Pasadena_Quinlan