Product Details

SNP ID
rs10263610
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:196186 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCCTGCTTCTTGTGGTTTTGAAGCC[A/G]TCCTTCGTCAGACCTCAGCAAGGCG
Phenotype
MIM: 611061
Polymorphism
A/G, 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 Intron NP_064608.2
XM_017012450.1 Intron XP_016867939.1
XM_017012451.1 Intron XP_016867940.1
XM_017012452.1 Intron XP_016867941.1
XM_017012453.1 Intron XP_016867942.1
XM_017012454.1 Intron XP_016867943.1
XM_017012455.1 Intron XP_016867944.1

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