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WormBase Tree Display for Variation: WBVar00237173

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Name Class

WBVar00237173NamePublic_nameWBVar00237173
Other_namepas48949
R12H7.1a.2:c.112+62del
R12H7.1a.1:c.112+62del
HGVSgCHROMOSOME_X:g.13212605del
Sequence_detailsSMapS_parentSequenceR12H7
Flanking_sequencestagaacatcatccattctccatttctgcccgtatttttcatctcttgttttcccgtcatatccttacatcaaatttttttttcagatcggaaaaggcgctacgggcgccgtcacgacatgacttaggatgagtatgctattgtattatttcgcgagtgctgtgaagtcaatacagtttcacgtcgatgatgacattattgacaagcttaactactattacaccacagccattatcacaggtattcttttcttaaataaaatgtatcaaactttttgatgaaacatagcatactggtttacaaaaaacacatgaaagagaaccgaaaaggtttaaaatgaaaataaatcttcatgaattagtacccattaaccaaggaccaaggacttgctctccctttcattttgttacatttttgatcaaagatgtttccaatcaagcatgtgtttctgaaccgttgggaagtattgaaatagaaaaagtttgaaataaatgttttgaaggagcttgaaatcaaaaaatcatttgataaaatagacattgaaaaagaaattcaacattaattatggcaattttgaagccataaaaaaacacgtctcta
Mapping_targetR12H7
Type_of_mutationDeletionA
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004604From_analysisWGS_Pasadena_Quinlan
PersonWBPerson6900
AnalysisWGS_Pasadena_Quinlan
StatusLive
AffectsGeneWBGene00006749
TranscriptR12H7.1a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR12H7.1a.2:c.112+62del
Intron_number3/10
R12H7.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR12H7.1a.1:c.112+62del
Intron_number2/9
MethodWGS_Pasadena_Quinlan