Product Details

SNP ID
rs35428582
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:60436910 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAAAAACCTTTTAAAGAAGAAGAAG[A/G]TATTGAATTTTGACCCTGTCCAAAT
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C14orf39 PubMed Links

Gene Details

Gene
C14orf39
Gene Name
chromosome 14 open reading frame 39
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_174978.2 1772 Missense Mutation NP_777638.2
XM_011536690.2 1772 Missense Mutation XP_011534992.1
XM_011536703.2 1772 Intron XP_011535005.1
XM_011536704.1 1772 Intron XP_011535006.1
XM_017021247.1 1772 Missense Mutation XP_016876736.1
XM_017021248.1 1772 Missense Mutation XP_016876737.1
XM_017021249.1 1772 Missense Mutation XP_016876738.1
XM_017021250.1 1772 Missense Mutation XP_016876739.1
XM_017021251.1 1772 Missense Mutation XP_016876740.1

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