Product Details

SNP ID
rs200087866
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:45617 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCGCTGTGCCGGGAGAAGCCGCTGC[C/T]GGAGGTGGCGACGCTCACGCTGCGC
Phenotype
MIM: 611395
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FAM110C PubMed Links

Gene Details

Gene
FAM110C
Gene Name
family with sequence similarity 110 member C
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001077710.2 914 Missense Mutation NP_001071178.2
XM_011510372.2 914 Missense Mutation XP_011508674.1
XM_017004689.1 914 Missense Mutation XP_016860178.1
XM_017004690.1 914 Missense Mutation XP_016860179.1
XM_017004691.1 914 Missense Mutation XP_016860180.1
XM_017004692.1 914 Missense Mutation XP_016860181.1

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