Product Details

SNP ID
rs200962622
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:195601 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCAGAATTCCTCTCCCCCGGGGAGG[C/T]GGCCGTGGACTCCTATCCCAACTGG
Phenotype
MIM: 611061
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FAM20C PubMed Links

Gene Details

Gene
FAM20C
Gene Name
family with sequence similarity 20 member C
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020223.3 894 Missense Mutation GCG,GTG A218V NP_064608.2
XM_017012450.1 894 Missense Mutation GCG,GTG A218V XP_016867939.1
XM_017012451.1 894 Missense Mutation GCG,GTG A218V XP_016867940.1
XM_017012452.1 894 Missense Mutation GCG,GTG A218V XP_016867941.1
XM_017012453.1 894 Missense Mutation GCG,GTG A218V XP_016867942.1
XM_017012454.1 894 Missense Mutation GCG,GTG A218V XP_016867943.1
XM_017012455.1 894 Intron XP_016867944.1

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