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WormBase Tree Display for Variation: WBVar00109147

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Name Class

WBVar00109147EvidencePaper_evidenceWBPaper00030778
WBPaper00055507
NamePublic_nameWBVar00109147
Other_namecbs44668
cb44668Paper_evidenceWBPaper00055507
HGVSgchrII:g.4860314T>C
Sequence_detailsSMapS_parentSequencecb25.fpc0072a
Flanking_sequencesgctcaaatttttcgaaaaatcggaatttcgattccaaaattttcagaaat
Mapping_targetcb25.fpc0072a
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
RFLPReference_strain_digestRAATTYAcsI, ApoI, XapI209 85 72 44 41 38 35 34 34 34 27 26 24 22 19 19 18 17 17 16 15 15 10 10 10 9 9 9 8 8 8 8 8 8 7 7 7 7 6
TTCGAAAsuII, Bpu14I, BsiCI, Bsp119I, BspT104I, BstBI, Csp45I, LspI, NspV, SfuI514 127 115 84 59 58 27 16
TCGAEsaBC3I, TaqI, TthHB8I249 146 127 108 84 59 41 34 34 27 26 17 16 15 9 8
TCNNGAHpy178III, Hpy188III556 336 87 21
TCNGAHpy188I208 201 138 124 83 71 33 26 26 25 24 24 17
CAYNNNNRTGMslI, SmiMI590 410
AATTSse9I, TasI, Tsp509I, TspEI189 85 44 41 41 38 34 34 31 27 26 22 21 19 19 18 17 17 17 16 15 15 14 10 10 10 10 10 10 10 9 9 9 8 8 8 8 8 8 8 7 7 7 7 7 6 6
Polymorphic_strain_digestRAATTYAcsI, ApoI, XapI209 85 72 55 44 41 38 35 34 34 34 26 19 19 18 17 17 17 16 15 10 10 10 10 9 9 9 8 8 8 8 8 8 7 7 7 7 6 6
TTCGAAAsuII, Bpu14I, BsiCI, Bsp119I, BspT104I, BstBI, Csp45I, LspI, NspV, SfuI514 127 99 84 59 58 27 16 16
TCGAEsaBC3I, TaqI, TthHB8I249 146 127 100 84 59 43 41 34 27 26 17 16 15 8 8
TCNNGAHpy178III, Hpy188III538 336 87 21 18
TCNGAHpy188I272 208 138 124 116 26 26 25 24 24 17
CAYNNNNRTGMslI, SmiMI1000
AATTSse9I, TasI, Tsp509I, TspEI189 85 55 44 41 41 38 34 34 31 26 21 19 19 17 17 17 17 16 15 10 10 10 10 10 10 10 10 9 9 9 8 8 8 8 8 8 8 8 7 7 7 7 7 6 6 6
Natural_variant
OriginSpeciesCaenorhabditis briggsae
StrainWBStrain00041077
LaboratoryCP
PersonWBPerson3706
WBPerson227
WBPerson225
StatusLive
AffectsGeneWBGene00026966
WBGene00026969
TranscriptCBG04253a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG04253a.1:c.456+1119A>G
Intron_number4/22
CBG04253b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG04253b.1:c.456+1119A>G
Intron_number4/22
CBG04256.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG04256.1:c.427-73T>C
Intron_number4/5
ReferenceWBPaper00030778
WBPaper00055507
RemarkPredicted by: ssaha-SNP v2.0
This SNP was observed in 1 sequencing read(s)
MethodSNP