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WormBase Tree Display for Variation: WBVar01849320

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WBVar01849320	Name	Public_name	WBVar01849320
		Other_name (13)
		HGVSg	CHROMOSOME_X:g.7851025A>T
	Sequence_details	SMap	S_parent	Sequence	C54D2
		Flanking_sequences	CAGTCCCATTGGCATCATATAGAACTCCAT	GCCATAGATATGACATTGATACCTTAAAAT
		Mapping_target	C54D2
		Source_location	225	CHROMOSOME_X	7850975	7850975	From_analysis	Million_mutation_project_reanalysis
		Type_of_mutation	Substitution	A	T
		SeqStatus	Sequenced
	Variation_type	Natural_variant
	Origin	Species	Caenorhabditis elegans
		Strain	WBStrain00023018	From_analysis	Million_mutation_project_reanalysis
		Laboratory	VC
		Analysis	Million_mutation_project_reanalysis
		Status	Live
	Affects	Gene	WBGene00000367
		Transcript	C54D2.5a.1	VEP_consequence	synonymous_variant
				VEP_impact	LOW
				HGVSc	C54D2.5a.1:c.4377T>A
				HGVSp	CE30919:p.Ala1459=
				cDNA_position	4505
				CDS_position	4377
				Protein_position	1459
				Exon_number	26/32
				Codon_change	gcT/gcA
				Amino_acid_change	A
			C54D2.5g.1	VEP_consequence	synonymous_variant
				VEP_impact	LOW
				HGVSc	C54D2.5g.1:c.4443T>A
				HGVSp	CE50172:p.Ala1481=
				cDNA_position	4443
				CDS_position	4443
				Protein_position	1481
				Exon_number	24/29
				Codon_change	gcT/gcA
				Amino_acid_change	A
			C54D2.5a.2	VEP_consequence	synonymous_variant
				VEP_impact	LOW
				HGVSc	C54D2.5a.2:c.4377T>A
				HGVSp	CE30919:p.Ala1459=
				cDNA_position	4539
				CDS_position	4377
				Protein_position	1459
				Exon_number	27/33
				Codon_change	gcT/gcA
				Amino_acid_change	A
			C54D2.5c.1	VEP_consequence	synonymous_variant
				VEP_impact	LOW
				HGVSc	C54D2.5c.1:c.4422T>A
				HGVSp	CE36115:p.Ala1474=
				cDNA_position	4498
				CDS_position	4422
				Protein_position	1474
				Exon_number	25/31
				Codon_change	gcT/gcA
				Amino_acid_change	A
			C54D2.5a.3	VEP_consequence	synonymous_variant
				VEP_impact	LOW
				HGVSc	C54D2.5a.3:c.4377T>A
				HGVSp	CE30919:p.Ala1459=
				cDNA_position	4454
				CDS_position	4377
				Protein_position	1459
				Exon_number	25/31
				Codon_change	gcT/gcA
				Amino_acid_change	A
			C54D2.5d.1	VEP_consequence	synonymous_variant
				VEP_impact	LOW
				HGVSc	C54D2.5d.1:c.4521T>A
				HGVSp	CE36116:p.Ala1507=
				cDNA_position	4597
				CDS_position	4521
				Protein_position	1507
				Exon_number	26/32
				Codon_change	gcT/gcA
				Amino_acid_change	A
			C54D2.5e.1	VEP_consequence	synonymous_variant
				VEP_impact	LOW
				HGVSc	C54D2.5e.1:c.4398T>A
				HGVSp	CE36117:p.Ala1466=
				cDNA_position	4474
				CDS_position	4398
				Protein_position	1466
				Exon_number	25/31
				Codon_change	gcT/gcA
				Amino_acid_change	A
	Method	WGS_Flibotte