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WormBase Tree Display for Variation: WBVar01677915

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WBVar01677915	Name	Public_name	WBVar01677915
		Other_name	cewivar00368141
			T28F12.2h.1:c.342+219G>A
			T28F12.2d.3:c.-802+219G>A
			T28F12.2c.1:c.-1366+219G>A
			T28F12.2d.1:c.-784+219G>A
			T28F12.2e.1:c.453+219G>A
			T28F12.2f.1:c.564+219G>A
			T28F12.2d.2:c.-802+219G>A
			T28F12.2c.2:c.-982+219G>A
			T28F12.2d.6:c.-796+219G>A
			T28F12.2g.1:c.342+219G>A
			T28F12.2b.1:c.453+219G>A
			T28F12.2d.4:c.-784+219G>A
			T28F12.2d.5:c.-796+219G>A
			T28F12.2a.1:c.564+219G>A
		HGVSg	CHROMOSOME_V:g.4502243G>A
	Sequence_details	SMap	S_parent	Sequence	T28F12
		Flanking_sequences	ACCGTATCAGTGTGTTGAAGAGAGCTAGTT	AAAAAAGTGCATTTCTACGATTTTTGGTTT
		Mapping_target	T28F12
		Source_location	225	CHROMOSOME_V	4502229	4502229	From_analysis	Million_mutation_project_reanalysis
		Type_of_mutation	Substitution	G	A
		SeqStatus	Sequenced
	Variation_type	Natural_variant
	Origin	Species	Caenorhabditis elegans
		Strain	WBStrain00006637	From_analysis	Million_mutation_project_reanalysis
			WBStrain00023072	From_analysis	Million_mutation_project_reanalysis
		Laboratory	VC
		Analysis	Million_mutation_project_reanalysis
		Status	Live
	Affects	Gene	WBGene00006796
		Transcript	T28F12.2h.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T28F12.2h.1:c.342+219G>A
				Intron_number	3/8
			T28F12.2e.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T28F12.2e.1:c.453+219G>A
				Intron_number	4/9
			T28F12.2d.4	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T28F12.2d.4:c.-784+219G>A
				Intron_number	4/11
			T28F12.2d.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T28F12.2d.1:c.-784+219G>A
				Intron_number	4/11
			T28F12.2a.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T28F12.2a.1:c.564+219G>A
				Intron_number	5/11
			T28F12.2b.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T28F12.2b.1:c.453+219G>A
				Intron_number	5/11
			T28F12.2d.2	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T28F12.2d.2:c.-802+219G>A
				Intron_number	4/11
			T28F12.2d.5	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T28F12.2d.5:c.-796+219G>A
				Intron_number	3/10
			T28F12.2c.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T28F12.2c.1:c.-1366+219G>A
				Intron_number	4/10
			T28F12.2d.3	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T28F12.2d.3:c.-802+219G>A
				Intron_number	4/11
			T28F12.2d.6	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T28F12.2d.6:c.-796+219G>A
				Intron_number	1/8
			T28F12.2g.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T28F12.2g.1:c.342+219G>A
				Intron_number	3/8
			T28F12.2c.2	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T28F12.2c.2:c.-982+219G>A
				Intron_number	4/10
			T28F12.2f.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	T28F12.2f.1:c.564+219G>A
				Intron_number	5/10
	Method	WGS_Flibotte