Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar00062099

expand all nodes | collapse all nodes | view schema

Name Class

WBVar00062099NamePublic_nameWBVar00062099
Other_namepas24017
haw106534
cewivar00060829
T06H11.1g.1:c.1153+140T>C
T06H11.1f.1:c.1468+140T>C
T06H11.1c.1:c.1204+140T>C
T06H11.1b.1:c.1279+140T>C
T06H11.1d.1:c.1348+140T>C
T06H11.1a.1:c.1393+140T>C
T06H11.1e.1:c.1123+140T>C
HGVSgCHROMOSOME_X:g.10105925A>G
Sequence_detailsSMapS_parentSequenceT06H11
Flanking_sequencesggacgcaagatccacgcacatggtcactacggaaagacctgaaagaaaaatttgtttcctaactcggctattttataccacaaaatttcaaaatgaaaatatttatcatgtattccattgttattccaccgttcgattgttgaaaaattattttttaaatcttattttaagccttgacaatctgaatataaataaactctaaaatattgcacaaatatttgccgttcatcagtattctctgtttttcacttttatactaagtgtccaaatactttttgagaataacgaagttcataaaattctttcaacattacaattttcaactttcaaattaacagtcattttaccataatttgattattatcatggtttccatgttagttttcttttgctaattatgaaaaaagagtttccaatatgaaaatagatgttaactcaccaactatcacaaatgcaacgataagtgataaaaatatgtaatcagtcacaacgatatctccgagtccgactgttacaatcaaattgaaaccaaaatgaaacgcatgaatgaaagaccaagttctagaagattatagtacacaaatattcaaaaaaccttga
Mapping_targetT06H11
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (19)
LaboratoryRW
PersonWBPerson6900
WBPerson1562
AnalysisWGS_Pasadena_Quinlan
Million_mutation_project_reanalysis
WGS_Hawaiian_Waterston
HistoryAcquires_mergeWBVar00082174
StatusLive
AffectsGeneWBGene00006792
TranscriptT06H11.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1b.1:c.1279+140T>C
Intron_number10/12
T06H11.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1g.1:c.1153+140T>C
Intron_number9/12
T06H11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1f.1:c.1468+140T>C
Intron_number12/14
T06H11.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1e.1:c.1123+140T>C
Intron_number10/13
T06H11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1d.1:c.1348+140T>C
Intron_number9/11
T06H11.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1a.1:c.1393+140T>C
Intron_number8/11
T06H11.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1c.1:c.1204+140T>C
Intron_number10/13
MethodWGS_Pasadena_Quinlan