Product Details

SNP ID
rs141229300
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:25315358 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTGCTGCCCGAGAAGCTCATAACC[A/G]AAGATGTCAGCCTCCCCTGTCCCGA
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_001318148.1 202 Missense Mutation CAA,CGA Q96R NP_001305077.1
NM_024936.2 202 Missense Mutation CAA,CGA Q96R NP_079212.2
XM_011513835.1 202 Missense Mutation CAA,CGA Q96R XP_011512137.1
XM_017008128.1 202 Missense Mutation CAA,CGA Q51R XP_016863617.1
XM_017008129.1 202 Missense Mutation CAA,CGA Q96R XP_016863618.1

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