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WormBase Tree Display for Variation: WBVar00064634

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Name Class

WBVar00064634EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar00064634
Other_namepas24524
haw107187
cewivar00061548
F31B12.1k.1:c.1958-34A>C
F31B12.1l.1:c.1787-34A>C
F31B12.1g.1:c.1787-34A>C
F31B12.1i.1:c.1958-34A>C
F31B12.1h.1:c.1787-34A>C
F31B12.1j.1:c.1787-34A>C
F31B12.1d.1:c.1958-34A>C
HGVSgCHROMOSOME_X:g.10824725T>G
Sequence_detailsSMapS_parentSequenceF31B12
Flanking_sequencesaagttggttctaacaaagctaccaagcttctgagctgatgtcgttcagacaaccgacttcgaaattttctgtaaaattttttgatctcatcaaatttcattttctcatcaaattactttgcgtgtgttaagaatagcaataatctggccaccaatatctgtgtacaatgagcacaacactgcctccatcgatgagccggactacaaacagatcttgaccctacttcccggttttgcattgttatcgcgttgtgcaaggccacaatgactaaaatggaaaacatcttgtttttagtgtaaattttgaatgtttgcaagcaagcaaacaacacacaaaccctggcttggatccatttcgctgaaagaattcattaagtcggacttgtgtcgagttggtgccaccgtaggagaaggtaataacgattggtctctagaaaacagaaggctgttattaaatgttgaatgtgactaggtattacttatagccagctccgtaaatgaaaacatgatcgacagttgagttttggtctgcatttgagttgaaagattcgccagctgaaataaatgtgttttgaaaaaaacttgaagcttcgtctcggtg
Mapping_targetF31B12
Type_of_mutationSubstitutionTG
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (192)
LaboratoryQX
RW
PersonWBPerson6900
WBPerson1730
WBPerson1562
AnalysisWGS_Pasadena_Quinlan
Million_mutation_project_reanalysis
WGS_Hawaiian_Waterston
WGS_Andersen
HistoryAcquires_mergeWBVar00082827
WBVar01470957
StatusLive
AffectsGeneWBGene00004036
TranscriptF31B12.1j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1j.1:c.1787-34A>C
Intron_number17/63
F31B12.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1g.1:c.1787-34A>C
Intron_number17/63
F31B12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1d.1:c.1958-34A>C
Intron_number18/64
F31B12.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1h.1:c.1787-34A>C
Intron_number17/63
F31B12.1l.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1l.1:c.1787-34A>C
Intron_number17/63
F31B12.1i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1i.1:c.1958-34A>C
Intron_number18/64
F31B12.1k.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1k.1:c.1958-34A>C
Intron_number18/64
ReferenceWBPaper00040707
MethodWGS_Pasadena_Quinlan