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WormBase Tree Display for Variation: WBVar00096413

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WBVar00096413	Evidence	Paper_evidence	WBPaper00037807
	Name	Public_name	WBVar00096413
		Other_name	pas1272
			haw74047
			cewivar00046990
			W08A12.1c.1:c.123+311G>A
			W08A12.1a.1:c.47+311G>A
			W08A12.1b.3:c.141+311G>A
			W08A12.1b.1:c.141+311G>A
			W08A12.1b.2:c.141+311G>A
			W08A12.1e.1:c.66+311G>A
		HGVSg	CHROMOSOME_V:g.3692369G>A
	Sequence_details	SMap	S_parent	Sequence	W08A12
		Flanking_sequences	tttctcgaaaatatggctaccgtacctcttgatcttttgatcctttgttcacaccggcgctaataacactacagttggtcttggcattttgccaagcggaatgacatcactttcgccgtgtcagagtgtcccatttcggcttgatctacgtagatctacaaaaaatgcggcagagtactcaactgatttcgtatggtcaagaacgtgctgacgtcatcatatattttaaggaaaaaattcccgcattttttgtagatcaaaccgtgatgggacaacctggtatcaccttttacagtgtac	tataatcttattgcatagcggcattttttacttatttccgtttttttttcacttcttctacatttttttcatacaataatagaattttaaatacctccacacactgaataaataagatgtttttttttcactctgttccctcagtgctgctaaaaacacaaaacgaaaacatgttgtgttttccatgtttttctcacttgaatgttcgccggtgttggtttttgaactgttaggctccgccccaatgttctcttccgcttgataaggatgattgttcctgtcccatgtcgaggtccgaat
		Mapping_target	W08A12
		Type_of_mutation	Substitution	G	A
		SeqStatus	Sequenced
	Variation_type	SNP
		Predicted_SNP
		Natural_variant
	Origin	Species	Caenorhabditis elegans
		Strain (42)
		Laboratory	AX
			RW
		Person	WBPerson6900
			WBPerson1562
		Analysis	WGS_Pasadena_Quinlan
			WGS_De_Bono
			Million_mutation_project_reanalysis
			WGS_Hawaiian_Waterston
		History	Acquires_merge	WBVar00206771
				WBVar01274792
		Status	Live
	Affects	Gene	WBGene00021078
		Transcript	W08A12.1b.3	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	W08A12.1b.3:c.141+311G>A
				Intron_number	3/7
			W08A12.1a.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	W08A12.1a.1:c.47+311G>A
				Intron_number	2/7
			W08A12.1c.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	W08A12.1c.1:c.123+311G>A
				Intron_number	3/7
			W08A12.1b.2	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	W08A12.1b.2:c.141+311G>A
				Intron_number	4/8
			W08A12.1b.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	W08A12.1b.1:c.141+311G>A
				Intron_number	4/8
			W08A12.1e.1	VEP_consequence	intron_variant
				VEP_impact	MODIFIER
				HGVSc	W08A12.1e.1:c.66+311G>A
				Intron_number	1/4
	Reference	WBPaper00037807
	Method	WGS_Pasadena_Quinlan