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WormBase Tree Display for Variation: WBVar01655575

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WBVar01655575	Name	Public_name	WBVar01655575
		Other_name	cewivar00343136
			Y46E12BL.4d.1:c.256-178A>C
			Y46E12BL.4e.1:c.946-178A>C
			Y46E12BL.4i.1:c.898-178A>C
			Y46E12BL.4h.1:c.1108-178A>C
			Y46E12BL.4f.1:c.757-178A>C
			Y46E12BL.4g.1:c.940-178A>C
			Y46E12BL.4a.1:c.757-178A>C
			Y46E12BL.4b.1:c.763-178A>C
			Y46E12BL.4c.1:c.1102-178A>C
		HGVSg	CHROMOSOME_II:g.15225855A>C
	Sequence_details	SMap	S_parent	Sequence	Y46E12BL
		Flanking_sequences	AAATTTCGCCAGAAAAAATAGAAAAAATAC	TTTTTTTTTTCATTGAAAAATATTTATTTA
		Mapping_target	Y46E12BL
		Source_location	225	CHROMOSOME_II	15225779	15225779	From_analysis	Million_mutation_project_reanalysis
		Type_of_mutation	Substitution	A	C
		SeqStatus	Sequenced
	Variation_type	Natural_variant
	Origin	Species	Caenorhabditis elegans
		Strain	WBStrain00006631	From_analysis	Million_mutation_project_reanalysis
			WBStrain00022850	From_analysis	Million_mutation_project_reanalysis
			WBStrain00023072	From_analysis	Million_mutation_project_reanalysis
		Laboratory	VC
		Analysis	Million_mutation_project_reanalysis
		Status	Live
	Affects	Gene	WBGene00021597
		Transcript	Y46E12BL.4h.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	Y46E12BL.4h.1:c.1108-178A>C
				Intron_number	4/5
			Y46E12BL.4f.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	Y46E12BL.4f.1:c.757-178A>C
				Intron_number	4/5
			Y46E12BL.4i.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	Y46E12BL.4i.1:c.898-178A>C
				Intron_number	6/7
			Y46E12BL.4d.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	Y46E12BL.4d.1:c.256-178A>C
				Intron_number	2/3
			Y46E12BL.4c.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	Y46E12BL.4c.1:c.1102-178A>C
				Intron_number	5/7
			Y46E12BL.4b.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	Y46E12BL.4b.1:c.763-178A>C
				Intron_number	4/6
			Y46E12BL.4e.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	Y46E12BL.4e.1:c.946-178A>C
				Intron_number	4/5
			Y46E12BL.4a.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	Y46E12BL.4a.1:c.757-178A>C
				Intron_number	4/4
			Y46E12BL.4g.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	Y46E12BL.4g.1:c.940-178A>C
				Intron_number	4/5
	Method	WGS_Flibotte