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WormBase Tree Display for Variation: WBVar01729840

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WBVar01729840	Name	Public_name	WBVar01729840
		Other_name	cewivar00428365
			B0496.3f.1:c.113-1206C>T
			B0496.3e.1:c.830-1206C>T
			B0496.3a.2:c.113-1206C>T
			B0496.3b.1:c.113-1206C>T
			B0496.3a.1:c.113-1206C>T
			B0496.3h.2:c.113-1206C>T
			B0496.3g.1:c.113-1206C>T
			B0496.3d.1:c.113-1206C>T
			B0496.3h.1:c.113-1206C>T
		HGVSg	CHROMOSOME_IV:g.7430659C>T
	Sequence_details	SMap	S_parent	Sequence	B0496
		Flanking_sequences	AATGAAGAGAGAGTGAGAGATCCTCCAACT	GTCGCAAAGAAGTTTCTTTTTCGGACAAAC
		Mapping_target	B0496
		Source_location	225	CHROMOSOME_IV	7430648	7430648	From_analysis	Million_mutation_project_reanalysis
		Type_of_mutation	Substitution	C	T
		SeqStatus	Sequenced
	Variation_type	Natural_variant
	Origin	Species	Caenorhabditis elegans
		Strain	WBStrain00023139	From_analysis	Million_mutation_project_reanalysis
			WBStrain00027648	From_analysis	Million_mutation_project_reanalysis
			WBStrain00027660	From_analysis	Million_mutation_project_reanalysis
			WBStrain00027662	From_analysis	Million_mutation_project_reanalysis
		Laboratory	VC
		Analysis	Million_mutation_project_reanalysis
		Status	Live
	Affects	Gene	WBGene00006814
		Transcript	B0496.3h.2	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	B0496.3h.2:c.113-1206C>T
				Intron_number	1/27
			B0496.3a.2	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	B0496.3a.2:c.113-1206C>T
				Intron_number	2/27
			B0496.3b.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	B0496.3b.1:c.113-1206C>T
				Intron_number	1/30
			B0496.3g.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	B0496.3g.1:c.113-1206C>T
				Intron_number	4/31
			B0496.3a.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	B0496.3a.1:c.113-1206C>T
				Intron_number	7/32
			B0496.3e.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	B0496.3e.1:c.830-1206C>T
				Intron_number	7/34
			B0496.3f.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	B0496.3f.1:c.113-1206C>T
				Intron_number	1/28
			B0496.3h.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	B0496.3h.1:c.113-1206C>T
				Intron_number	4/30
			B0496.3d.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	B0496.3d.1:c.113-1206C>T
				Intron_number	4/32
	Method	WGS_Flibotte