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WormBase Tree Display for Variation: WBVar01607002

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WBVar01607002	Name	Public_name	WBVar01607002
		Other_name	cewivar00285502
			T08A11.1a.1:c.4181-149T>A
			T08A11.1d.1:c.4193-149T>A
			T08A11.1f.1:c.4187-143T>A
			T08A11.1g.1:c.4187-143T>A
			T08A11.1b.1:c.4187-149T>A
			T08A11.1c.1:c.4187-149T>A
			T08A11.1e.1:c.4181-143T>A
			T08A11.1h.1:c.4193-143T>A
		HGVSg	CHROMOSOME_III:g.4251153A>T
	Sequence_details	SMap	S_parent	Sequence	T08A11
		Flanking_sequences	TCAAAAATTCCAACCCCATTGTGCAAAAAA	TCGGGATTTGCTGTTAAAAAATTTATTTAC
		Mapping_target	T08A11
		Source_location	225	CHROMOSOME_III	4251126	4251126	From_analysis	Million_mutation_project_reanalysis
		Type_of_mutation	Substitution	A	T
		SeqStatus	Sequenced
	Variation_type	Natural_variant
	Origin	Species	Caenorhabditis elegans
		Strain	WBStrain00006622	From_analysis	Million_mutation_project_reanalysis
			WBStrain00022852	From_analysis	Million_mutation_project_reanalysis
			WBStrain00022856	From_analysis	Million_mutation_project_reanalysis
			WBStrain00022878	From_analysis	Million_mutation_project_reanalysis
			WBStrain00022886	From_analysis	Million_mutation_project_reanalysis
			WBStrain00023286	From_analysis	Million_mutation_project_reanalysis
		Laboratory	VC
		Analysis	Million_mutation_project_reanalysis
		Status	Live
	Affects	Gene	WBGene00011604
		Transcript	T08A11.1e.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T08A11.1e.1:c.4181-143T>A
				Intron_number	14/17
			T08A11.1g.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T08A11.1g.1:c.4187-143T>A
				Intron_number	15/18
			T08A11.1h.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T08A11.1h.1:c.4193-143T>A
				Intron_number	15/18
			T08A11.1d.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T08A11.1d.1:c.4193-149T>A
				Intron_number	15/18
			T08A11.1f.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T08A11.1f.1:c.4187-143T>A
				Intron_number	14/17
			T08A11.1c.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T08A11.1c.1:c.4187-149T>A
				Intron_number	14/17
			T08A11.1b.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T08A11.1b.1:c.4187-149T>A
				Intron_number	15/18
			T08A11.1a.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T08A11.1a.1:c.4181-149T>A
				Intron_number	15/18
	Method	WGS_Flibotte