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WormBase Tree Display for Variation: WBVar01795040

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WBVar01795040	Name	Public_name	WBVar01795040
		Other_name (17)
		HGVSg	CHROMOSOME_IV:g.9541459A>G
	Sequence_details	SMap	S_parent	Sequence	F56H11
		Flanking_sequences	TAAATGTTGTAATGGTGACATTGAAATCAC	CATGCTTCCGAGATCATAACTGGTAGGAAA
		Mapping_target	F56H11
		Source_location	225	CHROMOSOME_IV	9541442	9541442	From_analysis	Million_mutation_project_reanalysis
		Type_of_mutation	Substitution	A	G
		SeqStatus	Sequenced
	Variation_type	Natural_variant
	Origin	Species	Caenorhabditis elegans
		Strain	WBStrain00023286	From_analysis	Million_mutation_project_reanalysis
		Laboratory	VC
		Analysis	Million_mutation_project_reanalysis
		Status	Live
	Affects	Gene	WBGene00001403
		Transcript	F56H11.1e.1	VEP_consequence	synonymous_variant
				VEP_impact	LOW
				HGVSc	F56H11.1e.1:c.408A>G
				HGVSp	CE49972:p.Thr136=
				cDNA_position	408
				CDS_position	408
				Protein_position	136
				Exon_number	3/12
				Codon_change	acA/acG
				Amino_acid_change	T
			F56H11.1d.1	VEP_consequence	synonymous_variant
				VEP_impact	LOW
				HGVSc	F56H11.1d.1:c.408A>G
				HGVSp	CE49921:p.Thr136=
				cDNA_position	408
				CDS_position	408
				Protein_position	136
				Exon_number	3/12
				Codon_change	acA/acG
				Amino_acid_change	T
			F56H11.1a.1	VEP_consequence	synonymous_variant
				VEP_impact	LOW
				HGVSc	F56H11.1a.1:c.408A>G
				HGVSp	CE26701:p.Thr136=
				cDNA_position	452
				CDS_position	408
				Protein_position	136
				Exon_number	4/16
				Codon_change	acA/acG
				Amino_acid_change	T
			F56H11.1g.1	VEP_consequence	synonymous_variant
				VEP_impact	LOW
				HGVSc	F56H11.1g.1:c.408A>G
				HGVSp	CE49816:p.Thr136=
				cDNA_position	452
				CDS_position	408
				Protein_position	136
				Exon_number	4/16
				Codon_change	acA/acG
				Amino_acid_change	T
			F56H11.1h.1	VEP_consequence	synonymous_variant
				VEP_impact	LOW
				HGVSc	F56H11.1h.1:c.408A>G
				HGVSp	CE49885:p.Thr136=
				cDNA_position	408
				CDS_position	408
				Protein_position	136
				Exon_number	3/12
				Codon_change	acA/acG
				Amino_acid_change	T
			F56H11.1c.1	VEP_consequence	synonymous_variant
				VEP_impact	LOW
				HGVSc	F56H11.1c.1:c.408A>G
				HGVSp	CE38374:p.Thr136=
				cDNA_position	454
				CDS_position	408
				Protein_position	136
				Exon_number	4/16
				Codon_change	acA/acG
				Amino_acid_change	T
			F56H11.1f.1	VEP_consequence	synonymous_variant
				VEP_impact	LOW
				HGVSc	F56H11.1f.1:c.408A>G
				HGVSp	CE49772:p.Thr136=
				cDNA_position	408
				CDS_position	408
				Protein_position	136
				Exon_number	3/12
				Codon_change	acA/acG
				Amino_acid_change	T
			F56H11.1b.1	VEP_consequence	synonymous_variant
				VEP_impact	LOW
				HGVSc	F56H11.1b.1:c.408A>G
				HGVSp	CE26702:p.Thr136=
				cDNA_position	425
				CDS_position	408
				Protein_position	136
				Exon_number	4/16
				Codon_change	acA/acG
				Amino_acid_change	T
	Method	WGS_Flibotte