Product Details

SNP ID
rs199910536
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:70044615 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCTCGCCGGTGCCCTCGACCTGCC[A/C]GCTGGGTCCTGTGCCTTTGAAGAGA
Phenotype
MIM: 612879
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
MAMDC2 PubMed Links

Gene Details

Gene
MAMDC2
Gene Name
MAM domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_153267.4 745 Silent Mutation CCA,CCC P22P NP_694999.3
XM_011518471.1 745 Silent Mutation CCA,CCC P22P XP_011516773.1
XM_011518475.2 745 Silent Mutation CCA,CCC P22P XP_011516777.1
XM_017014587.1 745 Silent Mutation CCA,CCC P22P XP_016870076.1

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