Product Details

SNP ID
rs142617435
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:1338649 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGAGCAGGACCCAGGGAGTGCCAGC[A/G]CCGACCCGCAGGAGCCTGCCACGGG
Phenotype
MIM: 604009
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
BAIAP3 PubMed Links

Gene Details

Gene
BAIAP3
Gene Name
BAI1 associated protein 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199096.1 858 Missense Mutation ACC,GCC T34A NP_001186025.1
NM_001199097.1 858 Missense Mutation ACC,GCC T34A NP_001186026.1
NM_001199098.1 858 Missense Mutation ACC,GCC T34A NP_001186027.1
NM_001199099.1 858 Missense Mutation ACC,GCC T34A NP_001186028.1
NM_001286464.1 858 Missense Mutation ACC,GCC T34A NP_001273393.1
NM_003933.4 858 Missense Mutation ACC,GCC T69A NP_003924.2
XM_011522728.1 858 Missense Mutation ACC,GCC T69A XP_011521030.1
XM_011522729.1 858 Missense Mutation ACC,GCC T69A XP_011521031.1
XM_011522730.2 858 Missense Mutation ACC,GCC T69A XP_011521032.1

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