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WormBase Tree Display for Variation: WBVar00143992

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WBVar00143992	Evidence	Paper_evidence	WBPaper00006370
		Person_evidence	WBPerson625
	Name	Public_name	e1417
		Other_name	F36H1.4h.2:c.56-209C>T
			F36H1.4b.1:c.56-209C>T
			F36H1.4g.1:c.56-203C>T
			F36H1.4d.1:c.56-209C>T
			F36H1.4b.3:c.56-209C>T
			F36H1.4c.1:c.56-203C>T
			F36H1.4h.1:c.56-209C>T
			F36H1.4a.1:c.56-203C>T
			F36H1.4b.2:c.56-209C>T
			F36H1.4f.1:c.56-209C>T
		HGVSg	CHROMOSOME_IV:g.11059196C>T
	Sequence_details	SMap	S_parent	Sequence	F36H1
		Flanking_sequences	tgctggttttttcttgtgac	ctgaaaactgtacacacaggtg
		Mapping_target	F36H1
		Type_of_mutation	Substitution	C	T	Person_evidence	WBPerson625
		SeqStatus	Sequenced
	Variation_type	Allele
	Origin	Species	Caenorhabditis elegans
		Strain	WBStrain00004330
			WBStrain00026836
			WBStrain00040217
		Laboratory	CB
		Status	Live
	Affects	Gene	WBGene00002992
		Transcript	F36H1.4g.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	F36H1.4g.1:c.56-203C>T
				Intron_number	4/13
			F36H1.4b.3	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	F36H1.4b.3:c.56-209C>T
				Intron_number	2/10
			F36H1.4d.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	F36H1.4d.1:c.56-209C>T
				Intron_number	3/13
			F36H1.4f.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	F36H1.4f.1:c.56-209C>T
				Intron_number	1/10
			F36H1.4b.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	F36H1.4b.1:c.56-209C>T
				Intron_number	3/12
			F36H1.4c.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	F36H1.4c.1:c.56-203C>T
				Intron_number	4/13
			F36H1.4a.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	F36H1.4a.1:c.56-203C>T
				Intron_number	4/13
			F36H1.4h.2	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	F36H1.4h.2:c.56-209C>T
				Intron_number	3/12
			F36H1.4h.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	F36H1.4h.1:c.56-209C>T
				Intron_number	4/13
			F36H1.4b.2	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	F36H1.4b.2:c.56-209C>T
				Intron_number	4/13
		Interactor	WBInteraction000009223
			WBInteraction000500498
			WBInteraction000524354
			WBInteraction000524526
			WBInteraction000538539
			WBInteraction000538543
			WBInteraction000556184
	Isolation	Mutagen	EMS
		Forward_genetics	standard phenotypic screen
	Genetics	Interpolated_map_position	IV	4.82035
		Mapping_data	In_multi_point	117
				382
				383
				603
				678
				774
				1135
				1137
			In_pos_neg_data	834
				970
	Description (2)
	Reference (13)
	Remark	N2 tgctggttttttcttgtgaccctgaaaactgtacacacaggtg
	Method	Substitution_allele