Product Details

SNP ID
rs1950287
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:57994974 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ACCTTAAGCATGAACAGAAATGTGT[C/G]CTAAAAAGCCTGGTCTTTCCAGTGA
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
C14orf37 PubMed Links

Gene Details

Gene
C14orf37
Gene Name
chromosome 14 open reading frame 37
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001001872.3 12165 Intron NP_001001872.2
NM_001320173.1 12165 Intron NP_001307102.1
XM_011536471.2 12165 Intron XP_011534773.1
XM_017021029.1 12165 UTR 3 XP_016876518.1
XM_017021030.1 12165 UTR 3 XP_016876519.1

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