Product Details

SNP ID
rs74936566
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.13:45962248 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTCTAATACAACCACCATAGCAGC[A/C]AAAATAGAAGAAGTCTGATTGTTAA
Phenotype
MIM: 616453
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
ZC3H13 PubMed Links

Gene Details

Gene
ZC3H13
Gene Name
zinc finger CCCH-type containing 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_005266301.3 6636 Intron XP_005266358.1
XM_005266302.3 6636 Intron XP_005266359.1
XM_005266303.3 6636 Intron XP_005266360.1
XM_005266304.3 6636 Intron XP_005266361.1
XM_005266305.3 6636 Intron XP_005266362.1
XM_005266306.3 6636 Intron XP_005266363.1
XM_005266307.3 6636 Intron XP_005266364.1
XM_005266308.3 6636 Intron XP_005266365.1
XM_005266309.3 6636 Intron XP_005266366.1
XM_005266310.3 6636 Intron XP_005266367.1
XM_005266311.3 6636 Intron XP_005266368.1
XM_005266312.1 6636 UTR 3 XP_005266369.1
XM_017020475.1 6636 Intron XP_016875964.1
XM_017020476.1 6636 Intron XP_016875965.1
XM_017020477.1 6636 Intron XP_016875966.1
XM_017020478.1 6636 Intron XP_016875967.1
XM_017020479.1 6636 Intron XP_016875968.1
XM_017020480.1 6636 Intron XP_016875969.1
XM_017020481.1 6636 Intron XP_016875970.1
XM_017020482.1 6636 Intron XP_016875971.1

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