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WormBase Tree Display for Variation: WBVar00012074

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Name Class

WBVar00012074EvidencePaper_evidenceWBPaper00030778
WBPaper00055507
NamePublic_nameWBVar00012074
Other_namecbs10557
cb10557Paper_evidenceWBPaper00055507
HGVSgchrV:g.18799292T>G
Sequence_detailsSMapS_parentSequencecb25.fpc0129
Flanking_sequencesgtaaaacaggcaaatttaaaaacttaacataaaaggtgatatgggttagt
Mapping_targetcb25.fpc0129
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
RFLPReference_strain_digestGTMKACAccI, FblI, XmiI916 84
TTTAAAAhaIII, DraI491 439 70
ACNGTBst4CI, HpyCH4III, TaaI, Tsp4CI500 283 156 61
CATGCviAII, FatI, HpyCH4I, Hsp92II, NlaIII267 243 204 135 93 38 20
TCGAEsaBC3I, TaqI, TthHB8I494 293 93 59 21 16 15 9
GTYRACHincII, HindII513 318 83 45 41
GTNNACHpy8I513 318 83 45 26 15
CGWCGHpy99I933 67
TTAAMseI, Tru1I, Tru9I274 177 164 99 99 84 61 33 9
GTCGACSalI915 85
Polymorphic_strain_digestGTMKACAccI, FblI, XmiI1000
TTTAAAAhaIII, DraI491 438 71
ACNGTBst4CI, HpyCH4III, TaaI, Tsp4CI500 283 217
CATGCviAII, FatI, HpyCH4I, Hsp92II, NlaIII263 243 204 135 93 38 20 4
TCGAEsaBC3I, TaqI, TthHB8I494 293 117 59 21 16
GTYRACHincII, HindII596 318 45 41
GTNNACHpy8I596 318 45 26 15
CGWCGHpy99I1000
TTAAMseI, Tru1I, Tru9I274 176 164 99 99 84 71 33
GTCGACSalI1000
Natural_variant
OriginSpeciesCaenorhabditis briggsae
StrainWBStrain00041077
LaboratoryCP
PersonWBPerson3706
WBPerson227
WBPerson225
StatusLive
AffectsGeneWBGene00027983
TranscriptCBG05555a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG05555a.1:c.5989-279A>C
Intron_number24/34
CBG05555b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG05555b.1:c.5883+137A>C
Intron_number23/32
CBG05555c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG05555c.1:c.5997+137A>C
Intron_number23/32
CBG05555d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG05555d.1:c.5821-279A>C
Intron_number21/30
CBG05555f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG05555f.1:c.*1557-279A>C
Intron_number23/30
CBG05555f.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG05555f.2:c.*1565+137A>C
Intron_number23/30
CBG05555f.3VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScCBG05555f.3:c.*1702A>C
cDNA_position6136
Exon_number23/23
ReferenceWBPaper00030778
WBPaper00055507
RemarkPredicted by: CrossMatch, Polybayes, ssaha-SNP v1.0, ssaha-SNP v2.0
This SNP was observed in 1 sequencing read(s)
MethodSNP