Product Details

SNP ID
rs200009932
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:121351169 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTTCAAAAGGGCTTTTTGTCTTAA[C/T]GCCCTTCCCACCACAGAAGACCCAG
Phenotype
MIM: 608618
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FAM3C PubMed Links

Gene Details

Gene
FAM3C
Gene Name
family with sequence similarity 3 member C
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001040020.1 908 Intron NP_001035109.1
NM_014888.2 908 Intron NP_055703.1
XM_011515736.2 908 Intron XP_011514038.1
XM_011515737.2 908 Missense Mutation ATT,GTT I190V XP_011514039.1

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