Product Details

SNP ID
rs11539086
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:58566602 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCAGCTGGCCCTACAGCTCTCTCT[C/G]TTCGCTGGTCAGTGTGGCAATTCTC
Phenotype
MIM: 608295
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
FAM107A PubMed Links

Gene Details

Gene
FAM107A
Gene Name
family with sequence similarity 107 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001076778.2 1130 Missense Mutation CAG,GAG Q141E NP_001070246.1
NM_001282713.1 1130 Missense Mutation CAG,GAG Q169E NP_001269642.1
NM_001282714.1 1130 Missense Mutation CAG,GAG Q172E NP_001269643.1
NM_007177.3 1130 Missense Mutation CAG,GAG Q141E NP_009108.1

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