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WormBase Tree Display for Variation: WBVar00227682

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Name Class

WBVar00227682NamePublic_nameWBVar00227682
Other_namepas39458
cewivar00093109
T24H10.7h.1:c.509+970T>C
T24H10.7i.1:c.398+970T>C
T24H10.7g.1:c.275+970T>C
T24H10.7f.1:c.551+970T>C
T24H10.7b.1:c.647+970T>C
T24H10.7a.1:c.707+970T>C
HGVSgCHROMOSOME_II:g.9124306T>C
Sequence_detailsSMapS_parentSequenceT24H10
Flanking_sequencestaattgggtagaaacattgcaatttaaaatttgaagttttatgaaaaaattgtgtaccgtattcttttttatttgcaaatgtgggtcctgttcttttgcctacaagttataaaaatactttcaagaaagtcgagagctctcagttaccaccaaaaagtttacttttgaaaatttgaaagctatattctgttggaaaagtttgaacagcagacacctgtcagatttcgcaacactgtccttttttgtataataaacctcttagtactggtcaaacaaaaaagtcaagattaagtgcaagaactgcataatcttttttgcaacaaaaaactagttcatccattcaaagttgcaacatttccaattccacccactcttttgaaattcaattgctatatatcacctgcctccctgcagtctatattcatttttctacccttgaacttctttcatttgcaagaattatctgtctgttctgttttcataggccaccctcctagatgatgatgatggtgactaagcattaaaactggaagttagataacgatttgactcatacagttcctaccagaatgaccctgaatatgagtcatctggaataaa
Mapping_targetT24H10
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000034From_analysisMillion_mutation_project_reanalysis
WBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00004604From_analysisWGS_Pasadena_Quinlan
WBStrain00006625From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
PersonWBPerson6900
AnalysisWGS_Pasadena_Quinlan
Million_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00012005
TranscriptT24H10.7g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7g.1:c.275+970T>C
Intron_number2/3
T24H10.7f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7f.1:c.551+970T>C
Intron_number6/8
T24H10.7i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7i.1:c.398+970T>C
Intron_number3/4
T24H10.7h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7h.1:c.509+970T>C
Intron_number4/5
T24H10.7a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7a.1:c.707+970T>C
Intron_number7/9
T24H10.7b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7b.1:c.647+970T>C
Intron_number7/9
MethodWGS_Pasadena_Quinlan