Product Details

SNP ID
rs2259365
Assay Type
Functionally Tested
NCBI dbSNP Submissions
5
Location
Chr.10:45768528 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTCTGGAGTCTAGAGTCTTACAAA[T/C]CAAAGTGGAGTCCACAAGCCAGCAG
Phenotype
MIM: 613631
Polymorphism
T/C, Transition Substitution
Allele Nomenclature
Literature Links
FAM21C PubMed Links

Gene Details

Gene
FAM21C
Gene Name
family with sequence similarity 21 member C
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001169106.1 Intron NP_001162577.1
NM_001169107.1 Intron NP_001162578.1
NM_015262.2 Intron NP_056077.2
XM_011539566.1 Intron XP_011537868.1
XM_011539567.1 Intron XP_011537869.1
XM_011539568.1 Intron XP_011537870.1
XM_011539569.1 Intron XP_011537871.1
XM_011539570.2 Intron XP_011537872.1
XM_011539571.1 Intron XP_011537873.1
XM_011539572.1 Intron XP_011537874.1
XM_011539573.2 Intron XP_011537875.1
XM_017016014.1 Intron XP_016871503.1
XM_017016015.1 Intron XP_016871504.1
XM_017016016.1 Intron XP_016871505.1
XM_017016017.1 Intron XP_016871506.1
XM_017016018.1 Intron XP_016871507.1
XM_017016019.1 Intron XP_016871508.1
XM_017016020.1 Intron XP_016871509.1
XM_017016021.1 Intron XP_016871510.1
XM_017016022.1 Intron XP_016871511.1
XM_017016023.1 Intron XP_016871512.1
XM_017016024.1 Intron XP_016871513.1
XM_017016025.1 Intron XP_016871514.1
XM_017016026.1 Intron XP_016871515.1

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