Product Details

SNP ID

rs137965903

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:119651700 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATGAGCGCCGCCACCCACTCGCCC[A/G]TGATGCAGGTGGCGTCCGGCAACGG

Phenotype

MIM: 603883

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

BAG3 PubMed Links

Gene Details

Gene

BAG3

Gene Name

BCL2 associated athanogene 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004281.3	331	Missense Mutation	ATG,GTG	M9V	NP_004272.2
XM_005270287.1	331	Missense Mutation	ATG,GTG	M9V	XP_005270344.1

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