Product Details

SNP ID
rs3764591
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:3370113 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TAGGTTCTTAGAGGGAGCTTGGGGG[G/T]TGCCTACCAGGAGCAGGGGGCCTGC
Phenotype
MIM: 600729
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
NFIC PubMed Links

Gene Details

Gene
NFIC
Gene Name
nuclear factor I C
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001245002.1 Intron NP_001231931.1
NM_001245004.1 Intron NP_001231933.1
NM_001245005.1 Intron NP_001231934.1
NM_005597.3 Intron NP_005588.2
NM_205843.2 Intron NP_995315.1
XM_005259564.3 Intron XP_005259621.1
XM_006722759.2 Intron XP_006722822.2
XM_017026834.1 Intron XP_016882323.1
XM_017026835.1 Intron XP_016882324.1
XM_017026836.1 Intron XP_016882325.1

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