Product Details

SNP ID
rs199598617
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:25312870 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCAGAGGGCAGCGCAGGGTGCCGG[A/G]GAAGCTCGGGAATGGAGGTGGTGCT
Phenotype
MIM: 611792
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
ZCCHC4 PubMed Links

Gene Details

Gene
ZCCHC4
Gene Name
zinc finger CCHC-type containing 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318148.1 95 Missense Mutation AGA,GGA R21G NP_001305077.1
NM_024936.2 95 Missense Mutation AGA,GGA R21G NP_079212.2
XM_011513835.1 95 Missense Mutation AGA,GGA R21G XP_011512137.1
XM_017008128.1 95 Silent Mutation GGA,GGG G15G XP_016863617.1
XM_017008129.1 95 Missense Mutation AGA,GGA R21G XP_016863618.1

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