Product Details

SNP ID

rs189051470

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:17638829 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTCACCGCCGCTGGGGGACCCTGT[C/T]GGAAGCAACTGCCGCCGCCGCCTCT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

BCL2L13 PubMed Links

Gene Details

Gene

BCL2L13

Gene Name

BCL2 like 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001270726.1	780	Missense Mutation	CGG,TGG	R46W	NP_001257655.1
NM_001270727.1	780	Missense Mutation	CGG,TGG	R46W	NP_001257656.1
NM_001270728.1	780	UTR 5			NP_001257657.1
NM_001270729.1	780	UTR 5			NP_001257658.1
NM_001270730.1	780	UTR 5			NP_001257659.1
NM_001270731.1	780	UTR 5			NP_001257660.1
NM_001270732.1	780	UTR 5			NP_001257661.1
NM_001270733.1	780	Intron			NP_001257662.1
NM_001270734.1	780	UTR 5			NP_001257663.1
NM_001270735.1	780	UTR 5			NP_001257664.1
NM_015367.3	780	UTR 5			NP_056182.2
XM_011546119.1	780	Missense Mutation	CGG,TGG	R46W	XP_011544421.1
XM_011546120.1	780	Missense Mutation	CGG,TGG	R46W	XP_011544422.1
XM_011546121.2	780	Intron			XP_011544423.1
XM_011546123.1	780	UTR 5			XP_011544425.1
XM_017028725.1	780	Missense Mutation	CGG,TGG	R46W	XP_016884214.1
XM_017028726.1	780	UTR 5			XP_016884215.1
XM_017028727.1	780	UTR 5			XP_016884216.1
XM_017028728.1	780	UTR 5			XP_016884217.1
XM_017028729.1	780	UTR 5			XP_016884218.1
XM_017028730.1	780	UTR 5			XP_016884219.1
XM_017028731.1	780	UTR 5			XP_016884220.1
XM_017028732.1	780	UTR 5			XP_016884221.1
XM_017028733.1	780	UTR 5			XP_016884222.1
XM_017028734.1	780	UTR 5			XP_016884223.1

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