Product Details

SNP ID
rs200066912
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:48329816 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGCCAGAGAAGTGTGGAGACGGAA[C/T]GCGAGGGCGAAAGCCAAGGCCAATG
Phenotype
MIM: 613906
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
H1FNT PubMed Links
Additional Information
For this assay, SNP(s) [rs1471997] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
H1FNT
Gene Name
H1 histone family member N, testis specific
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_181788.1 837 Silent Mutation AAC,AAT N175N NP_861453.1
Gene
ZNF641
Gene Name
zinc finger protein 641
There are no transcripts associated with this gene.

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