Product Details

SNP ID
rs60995653
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:50725853 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTATAATAGAATTTGCCTTTATTA[C/G]ACAACATAAGTTAACGAGTTAATGG
Phenotype
MIM: 608684
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
NIN PubMed Links

Gene Details

Gene
NIN
Gene Name
ninein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_016350.4 6334 UTR 3 NP_057434.4
NM_020921.3 6334 Intron NP_065972.3
NM_182944.2 6334 Intron NP_891989.2
NM_182946.1 6334 UTR 3 NP_891991.1
XM_011536817.1 6334 Intron XP_011535119.1
XM_011536819.2 6334 Intron XP_011535121.1
XM_011536822.1 6334 Intron XP_011535124.1
XM_011536823.2 6334 UTR 3 XP_011535125.1

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