Product Details

SNP ID
rs199842190
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.22:38087188 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGGACATGGAGGTCATGGAGGTCA[C/T]GGGGGTCACGGGGGTCATGGGATTC
Phenotype
MIM: 610409
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
BAIAP2L2 PubMed Links

Gene Details

Gene
BAIAP2L2
Gene Name
BAI1 associated protein 2 like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_025045.5 1621 Missense Mutation ATG,GTG M399V NP_079321.3
XM_005261751.4 1621 Missense Mutation ATG,GTG M399V XP_005261808.1
XM_011530379.2 1621 Missense Mutation ATG,GTG M399V XP_011528681.1
XM_011530380.2 1621 Missense Mutation ATG,GTG M381V XP_011528682.1
XM_011530381.2 1621 Missense Mutation ATG,GTG M380V XP_011528683.1
XM_011530382.2 1621 Missense Mutation ATG,GTG M380V XP_011528684.1
XM_011530383.2 1621 Missense Mutation ATG,GTG M375V XP_011528685.1
XM_011530384.2 1621 Missense Mutation ATG,GTG M369V XP_011528686.1
XM_011530386.2 1621 Missense Mutation ATG,GTG M204V XP_011528688.1
XM_011530387.2 1621 Missense Mutation ATG,GTG M204V XP_011528689.1
XM_011530388.2 1621 Missense Mutation ATG,GTG M192V XP_011528690.1
Gene
SLC16A8
Gene Name
solute carrier family 16 member 8
There are no transcripts associated with this gene.

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