Product Details

SNP ID
rs181751721
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:74436586 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAACACGCTGGAGGCTGCTCTCCGG[A/G]TGTTCCCACTGGGGACCCCAGGGTC
Phenotype
MIM: 614544
Polymorphism
A/G, 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 1230 Missense Mutation ACC,ATC T392I NP_001037834.2
XM_011525816.2 1230 Missense Mutation ACC,ATC T354I XP_011524118.1
XM_017025551.1 1230 Missense Mutation ACC,ATC T251I XP_016881040.1

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