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WormBase Tree Display for Variation: WBVar00109149

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Name Class

WBVar00109149EvidencePaper_evidenceWBPaper00030778
WBPaper00055507
NamePublic_nameWBVar00109149
Other_namecbs44670
cb44670Paper_evidenceWBPaper00055507
HGVSgchrII:g.4860353G>T
Sequence_detailsSMapS_parentSequencecb25.fpc0072a
Flanking_sequencesattttcagaaattcaaaaatttataaaaatcgaaaaattcaaaattttca
Mapping_targetcb25.fpc0072a
Type_of_mutationSubstitutionGT
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
RFLPReference_strain_digestRAATTYAcsI, ApoI, XapI209 111 85 44 41 38 34 34 34 30 27 26 22 19 19 18 17 17 16 15 15 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, SfuI553 127 84 76 59 58 27 16
TCGAEsaBC3I, TaqI, TthHB8I249 185 127 84 69 59 41 34 34 27 26 17 16 15 9 8
TCNNGAHpy178III, Hpy188III595 336 69
TCNGAHpy188I247 201 138 85 83 71 33 26 26 25 24 24 17
CAYNNNNRTGMslI, SmiMI551 449
AATTSse9I, TasI, Tsp509I, TspEI189 85 76 44 41 38 34 34 31 27 26 22 21 19 19 18 17 17 17 16 15 15 10 10 10 10 10 9 9 9 8 8 8 8 8 8 7 7 7 7 7 6 6 4 3
Polymorphic_strain_digestRAATTYAcsI, ApoI, XapI209 111 85 55 44 41 38 34 34 34 30 26 19 19 17 17 17 16 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, SfuI553 127 84 60 59 58 27 16 16
TCGAEsaBC3I, TaqI, TthHB8I249 185 127 84 61 59 43 41 34 27 26 17 16 15 8 8
TCNNGAHpy178III, Hpy188III577 336 69 18
TCNGAHpy188I272 247 138 116 85 26 26 25 24 24 17
CAYNNNNRTGMslI, SmiMI1000
AATTSse9I, TasI, Tsp509I, TspEI189 85 76 55 44 41 38 34 34 31 26 21 19 19 17 17 17 17 16 15 10 10 10 10 10 10 9 9 9 8 8 8 8 8 8 7 7 7 7 7 6 6 4 3
Natural_variant
OriginSpeciesCaenorhabditis briggsae
StrainWBStrain00041077
LaboratoryCP
PersonWBPerson3706
WBPerson227
WBPerson225
StatusLive
AffectsGeneWBGene00026966
WBGene00026969
TranscriptCBG04253a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG04253a.1:c.456+1080C>A
Intron_number4/22
CBG04253b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG04253b.1:c.456+1080C>A
Intron_number4/22
CBG04256.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG04256.1:c.427-34G>T
Intron_number4/5
ReferenceWBPaper00030778
WBPaper00055507
RemarkPredicted by: ssaha-SNP v2.0
This SNP was observed in 1 sequencing read(s)
MethodSNP