Product Details

SNP ID
rs8010478
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:50724577 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCTTCCTTTCCTTAAAAAAACACTT[C/T]GATGGTTCTTCATTGCCGACAGAAT
Phenotype
MIM: 608684
Polymorphism
C/T, Transition 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 7610 Intron NP_057434.4
NM_020921.3 7610 Intron NP_065972.3
NM_182944.2 7610 Intron NP_891989.2
NM_182946.1 7610 Intron NP_891991.1
XM_011536817.1 7610 Intron XP_011535119.1
XM_011536819.2 7610 Intron XP_011535121.1
XM_011536822.1 7610 Intron XP_011535124.1
XM_011536823.2 7610 UTR 3 XP_011535125.1

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