Product Details

SNP ID
rs138249221
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:45618184 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGTCCTGTTTTCTTTCCACAAAG[A/C]AAACAATGATTTGTTGTTTTCTTCT
Phenotype
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
ZFAND4 PubMed Links

Gene Details

Gene
ZFAND4
Gene Name
zinc finger AN1-type containing 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001128324.2 2706 Missense Mutation TTG,TTT L668F NP_001121796.1
NM_001282905.1 2706 Missense Mutation TTG,TTT L594F NP_001269834.1
NM_001282906.1 2706 Missense Mutation TTG,TTT L594F NP_001269835.1
NM_174890.3 2706 Missense Mutation TTG,TTT L668F NP_777550.2
XM_005271842.2 2706 Missense Mutation TTG,TTT L569F XP_005271899.1
XM_005271843.2 2706 Missense Mutation TTG,TTT L569F XP_005271900.1
XM_005271844.3 2706 Missense Mutation TTG,TTT L550F XP_005271901.1
XM_011540366.2 2706 Missense Mutation TTG,TTT L676F XP_011538668.1
XM_011540368.1 2706 Missense Mutation TTG,TTT L496F XP_011538670.1
XM_017016931.1 2706 Missense Mutation TTG,TTT L682F XP_016872420.1
XM_017016932.1 2706 Missense Mutation TTG,TTT L674F XP_016872421.1
XM_017016933.1 2706 Missense Mutation TTG,TTT L674F XP_016872422.1
XM_017016934.1 2706 Missense Mutation TTG,TTT L674F XP_016872423.1
XM_017016935.1 2706 UTR 3 XP_016872424.1
XM_017016936.1 2706 Missense Mutation TTG,TTT L626F XP_016872425.1
XM_017016937.1 2706 Missense Mutation TTG,TTT L626F XP_016872426.1
XM_017016938.1 2706 Missense Mutation TTG,TTT L620F XP_016872427.1
XM_017016939.1 2706 Missense Mutation TTG,TTT L620F XP_016872428.1
XM_017016940.1 2706 Missense Mutation TTG,TTT L600F XP_016872429.1
XM_017016941.1 2706 Missense Mutation TTG,TTT L600F XP_016872430.1
XM_017016942.1 2706 Missense Mutation TTG,TTT L575F XP_016872431.1
XM_017016943.1 2706 Missense Mutation TTG,TTT L575F XP_016872432.1
XM_017016944.1 2706 Missense Mutation TTG,TTT L575F XP_016872433.1
XM_017016945.1 2706 Missense Mutation TTG,TTT L556F XP_016872434.1
XM_017016946.1 2706 Missense Mutation TTG,TTT L475F XP_016872435.1

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