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WormBase Tree Display for Variation: WBVar00135782

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WBVar00135782	Name	Public_name	WBVar00135782
		Other_name	cbh40308
		HGVSg	chrV:g.4371850G>A
	Sequence_details	SMap	S_parent	Sequence	cb25.fpc0023
		Flanking_sequences	GCTGTGTTCGGGGAGCCCAGAAAGG	CCTATTCATGAGTGGATTTTTGGTT
		Mapping_target	cb25.fpc0023
		Type_of_mutation	Substitution	C	T
		SeqStatus	Sequenced
	Variation_type	SNP
		Predicted_SNP
		Natural_variant
	Origin	Species	Caenorhabditis briggsae
		Strain	WBStrain00041078
		Laboratory	CP
		Person	WBPerson3706
			WBPerson227
			WBPerson225
		Status	Live
	Affects	Gene	WBGene00024561
		Transcript	CBG01302.1	VEP_consequence	missense_variant
				VEP_impact	MODERATE
				HGVSc	CBG01302.1:c.641C>T
				HGVSp	CBP35139.1:p.Ala214Val
				cDNA_position	2268
				CDS_position	641
				Protein_position	214
				Exon_number	10/12
				Codon_change	gCc/gTc
				Amino_acid_change	A/V
			CBG01302.2	VEP_consequence	missense_variant
				VEP_impact	MODERATE
				HGVSc	CBG01302.2:c.641C>T
				HGVSp	CBP35139.1:p.Ala214Val
				cDNA_position	2224
				CDS_position	641
				Protein_position	214
				Exon_number	10/12
				Codon_change	gCc/gTc
				Amino_acid_change	A/V
			CBG01302.3	VEP_consequence	missense_variant
				VEP_impact	MODERATE
				HGVSc	CBG01302.3:c.641C>T
				HGVSp	CBP35139.1:p.Ala214Val
				cDNA_position	2203
				CDS_position	641
				Protein_position	214
				Exon_number	9/11
				Codon_change	gCc/gTc
				Amino_acid_change	A/V
			CBG01302.4	VEP_consequence	missense_variant
				VEP_impact	MODERATE
				HGVSc	CBG01302.4:c.641C>T
				HGVSp	CBP35139.1:p.Ala214Val
				cDNA_position	2184
				CDS_position	641
				Protein_position	214
				Exon_number	9/11
				Codon_change	gCc/gTc
				Amino_acid_change	A/V
			CBG01302.5	VEP_consequence	missense_variant
				VEP_impact	MODERATE
				HGVSc	CBG01302.5:c.641C>T
				HGVSp	CBP35139.1:p.Ala214Val
				cDNA_position	2159
				CDS_position	641
				Protein_position	214
				Exon_number	9/11
				Codon_change	gCc/gTc
				Amino_acid_change	A/V
			CBG01302.6	VEP_consequence	missense_variant
				VEP_impact	MODERATE
				HGVSc	CBG01302.6:c.641C>T
				HGVSp	CBP35139.1:p.Ala214Val
				cDNA_position	2315
				CDS_position	641
				Protein_position	214
				Exon_number	9/11
				Codon_change	gCc/gTc
				Amino_acid_change	A/V
			CBG01302.7	VEP_consequence	missense_variant
				VEP_impact	MODERATE
				HGVSc	CBG01302.7:c.641C>T
				HGVSp	CBP35139.1:p.Ala214Val
				cDNA_position	2296
				CDS_position	641
				Protein_position	214
				Exon_number	9/11
				Codon_change	gCc/gTc
				Amino_acid_change	A/V
			CBG01302.8	VEP_consequence	missense_variant
				VEP_impact	MODERATE
				HGVSc	CBG01302.8:c.641C>T
				HGVSp	CBP35139.1:p.Ala214Val
				cDNA_position	2271
				CDS_position	641
				Protein_position	214
				Exon_number	9/11
				Codon_change	gCc/gTc
				Amino_acid_change	A/V
			CBG01302.9	VEP_consequence	missense_variant
				VEP_impact	MODERATE
				HGVSc	CBG01302.9:c.641C>T
				HGVSp	CBP35139.1:p.Ala214Val
				cDNA_position	2366
				CDS_position	641
				Protein_position	214
				Exon_number	8/10
				Codon_change	gCc/gTc
				Amino_acid_change	A/V
			CBG01302.10	VEP_consequence	missense_variant
				VEP_impact	MODERATE
				HGVSc	CBG01302.10:c.641C>T
				HGVSp	CBP35139.1:p.Ala214Val
				cDNA_position	2322
				CDS_position	641
				Protein_position	214
				Exon_number	8/10
				Codon_change	gCc/gTc
				Amino_acid_change	A/V
	Method	SNP