Product Details

SNP ID
rs75521739
Assay Type
Functionally Tested
NCBI dbSNP Submissions
14
Location
Chr.1:61084685 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGCAATAAAGGGAAAGGACCCTA[A/G]CAGATACATTAGTGTCTTCTCAATT
Phenotype
MIM: 600727
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
NFIA PubMed Links

Gene Details

Gene
NFIA
Gene Name
nuclear factor I A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001134673.3 Intron NP_001128145.1
NM_001145511.1 Intron NP_001138983.1
NM_001145512.1 Intron NP_001138984.1
NM_005595.4 Intron NP_005586.1
XM_011541512.2 Intron XP_011539814.1
XM_011541514.2 Intron XP_011539816.1
XM_011541515.2 Intron XP_011539817.1
XM_017001362.1 Intron XP_016856851.1
XM_017001363.1 Intron XP_016856852.1

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