Product Details

SNP ID
rs200669352
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:16963825 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACCGGAAACAGGAAATGCAGATGCC[A/G]GGTTCTGCTGTCACAAGGAGGAAAA
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
GAB4 PubMed Links

Gene Details

Gene
GAB4
Gene Name
GRB2 associated binding protein family member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001037814.1 882 Missense Mutation NP_001032903.1
XM_011546114.2 882 Missense Mutation XP_011544416.1
XM_011546115.1 882 Missense Mutation XP_011544417.1
XM_011546116.2 882 Intron XP_011544418.1
XM_011546117.1 882 Missense Mutation XP_011544419.1
XM_017028575.1 882 Missense Mutation XP_016884064.1
XM_017028576.1 882 Missense Mutation XP_016884065.1

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