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WormBase Tree Display for Variation: WBVar01553739

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WBVar01553739	Name	Public_name	WBVar01553739
		Other_name	cewivar00131053
			C03H12.1f.1:c.446+295T>C
			C03H12.1f.3:c.446+295T>C
			C03H12.1f.2:c.446+295T>C
			C03H12.1b.1:c.1649+133T>C
			C03H12.1e.1:c.1562+295T>C
			C03H12.1c.1:c.533+133T>C
			C03H12.1e.2:c.1562+295T>C
			C03H12.1a.1:c.1931+133T>C
			C03H12.1d.1:c.1844+295T>C
		HGVSg	CHROMOSOME_X:g.15695279T>C
	Sequence_details	SMap	S_parent	Sequence	ZK662
		Flanking_sequences	GCAAATTGATTTGTCGACAAATTCGGCTTG	CGGTTTGCCGATTTGCCGGAAATGTTCAAT
		Mapping_target	ZK662
		Source_location	225	CHROMOSOME_X	15695211	15695211	From_analysis	Million_mutation_project_reanalysis
		Type_of_mutation	Substitution	T	C
		SeqStatus	Sequenced
	Variation_type	Natural_variant
	Origin	Species	Caenorhabditis elegans
		Strain	WBStrain00004599	From_analysis	Million_mutation_project_reanalysis
			WBStrain00006622	From_analysis	Million_mutation_project_reanalysis
			WBStrain00006631	From_analysis	Million_mutation_project_reanalysis
			WBStrain00006643	From_analysis	Million_mutation_project_reanalysis
			WBStrain00006645	From_analysis	Million_mutation_project_reanalysis
			WBStrain00008273	From_analysis	Million_mutation_project_reanalysis
			WBStrain00023138	From_analysis	Million_mutation_project_reanalysis
		Laboratory	VC
		Analysis	Million_mutation_project_reanalysis
		Status	Live
	Affects	Gene	WBGene00007284
		Transcript	C03H12.1f.2	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C03H12.1f.2:c.446+295T>C
				Intron_number	6/8
			C03H12.1f.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C03H12.1f.1:c.446+295T>C
				Intron_number	11/13
			C03H12.1e.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C03H12.1e.1:c.1562+295T>C
				Intron_number	14/16
			C03H12.1b.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C03H12.1b.1:c.1649+133T>C
				Intron_number	13/14
			C03H12.1f.3	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C03H12.1f.3:c.446+295T>C
				Intron_number	5/7
			C03H12.1a.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C03H12.1a.1:c.1931+133T>C
				Intron_number	16/18
			C03H12.1c.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C03H12.1c.1:c.533+133T>C
				Intron_number	5/6
			C03H12.1d.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C03H12.1d.1:c.1844+295T>C
				Intron_number	15/17
			C03H12.1e.2	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C03H12.1e.2:c.1562+295T>C
				Intron_number	13/15
	Method	WGS_Flibotte