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WormBase Tree Display for Variation: WBVar00007891

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Name Class

WBVar00007891NamePublic_nameWBVar00007891
Other_namepas13175
T12B5.8.1:c.114-43C>G
T12B5.8.2:c.114-43C>G
HGVSgCHROMOSOME_III:g.941800G>C
Sequence_detailsSMapS_parentSequenceT12B5
Flanking_sequencestttttccgtgcgtgcttcgatactattttaaaatccttggcagctctttccataaagttttctccatcaatcaactttgtctgttcattgtgaaaaacattcgtactgccatttgctgttttagtatatatgatttcagtttcaccccaccatatttcgactttatctttcctcaagagaaaaacgatgacaccgaaacgtaatccaaattcatcgacagcagttctcaaactgcgacacacttttctcgcgctcagtctgtaacaaataactggttatttcagtgtggctatgatgttattttgaaaatttttctctattgctgttatattatgttgtgaaaaaagttttctccgaaatttcactccagttcattttctcattaactttattcttagtcactatcaatcaaccatataattatcattactattcacaactgtgagccacctattgggaggatcgtcgaccctcttcttccagaacgcgggcgagcgcgagtcgaagaagtcgttcactgccttttcgaggtcctcaaactttgcaaacttctgatctctaaggaacagcttgagcgggcggaaaggtgacaatccgaag
Mapping_targetT12B5
Type_of_mutationSubstitutionGC
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004604From_analysisWGS_Pasadena_Quinlan
PersonWBPerson6900
AnalysisWGS_Pasadena_Quinlan
StatusLive
AffectsGeneWBGene00020455
TranscriptT12B5.8.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT12B5.8.2:c.114-43C>G
Intron_number2/6
T12B5.8.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT12B5.8.1:c.114-43C>G
Intron_number2/5
MethodWGS_Pasadena_Quinlan