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WormBase Tree Display for Variation: WBVar01932250

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WBVar01932250	Name	Public_name	WBVar01932250
		Other_name	cewivar00651468
			C09D1.1n.1:c.795+1083_795+1084insAA
			C09D1.1m.1:c.795+1083_795+1084insAA
			C09D1.1f.1:c.795+1083_795+1084insAA
			C09D1.1l.1:c.795+1083_795+1084insAA
			C09D1.1o.1:c.795+1083_795+1084insAA
			C09D1.1b.1:c.795+1083_795+1084insAA
			C09D1.1e.1:c.795+1083_795+1084insAA
			C09D1.1k.1:c.795+1083_795+1084insAA
			C09D1.1a.1:c.795+1083_795+1084insAA
		HGVSg	CHROMOSOME_I:g.4039955_4039956insAA
	Sequence_details	SMap	S_parent	Sequence	C09D1
		Flanking_sequences	AAAACTTTGATTGAAAGTGTTGAAAAATCG	AAAAAAAAAACAATTTGAGCATTCTCATTC
		Mapping_target	C09D1
		Source_location	225	CHROMOSOME_I	4039957	4039958	From_analysis	Million_mutation_project_reanalysis
		Type_of_mutation	Insertion	AA
		SeqStatus	Sequenced
	Variation_type	Natural_variant
	Origin	Species	Caenorhabditis elegans
		Strain	WBStrain00000034	From_analysis	Million_mutation_project_reanalysis
			WBStrain00004599	From_analysis	Million_mutation_project_reanalysis
			WBStrain00006625	From_analysis	Million_mutation_project_reanalysis
			WBStrain00027662	From_analysis	Million_mutation_project_reanalysis
		Laboratory	VC
		Analysis	Million_mutation_project_reanalysis
		Status	Live
	Affects	Gene	WBGene00006820
		Transcript	C09D1.1b.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C09D1.1b.1:c.795+1083_795+1084insAA
				Intron_number	5/48
			C09D1.1o.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C09D1.1o.1:c.795+1083_795+1084insAA
				Intron_number	5/32
			C09D1.1k.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C09D1.1k.1:c.795+1083_795+1084insAA
				Intron_number	5/46
			C09D1.1l.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C09D1.1l.1:c.795+1083_795+1084insAA
				Intron_number	5/32
			C09D1.1n.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C09D1.1n.1:c.795+1083_795+1084insAA
				Intron_number	5/46
			C09D1.1a.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C09D1.1a.1:c.795+1083_795+1084insAA
				Intron_number	6/35
			C09D1.1e.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C09D1.1e.1:c.795+1083_795+1084insAA
				Intron_number	5/31
			C09D1.1f.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C09D1.1f.1:c.795+1083_795+1084insAA
				Intron_number	5/45
			C09D1.1m.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	C09D1.1m.1:c.795+1083_795+1084insAA
				Intron_number	5/47
	Method	WGS_Flibotte