Product Details

SNP ID
rs142666003
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:74436566 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGAGTTGGCGAAGCTTCCAGAACA[C/T]GCTGGAGGCTGCTCTCCGGGTGTTC
Phenotype
MIM: 614544
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FAM69C PubMed Links

Gene Details

Gene
FAM69C
Gene Name
family with sequence similarity 69 member C
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001044369.2 1250 Missense Mutation NP_001037834.2
XM_011525816.2 1250 Missense Mutation XP_011524118.1
XM_017025551.1 1250 Missense Mutation XP_016881040.1

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