Product Details

SNP ID

rs3810421

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:3365641 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCCATACCTCAGTCTTGAGATCTG[C/T]GAAAAGGGCACACCCCTGAGGCAGG

Phenotype

MIM: 600729

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NFIC PubMed Links

Additional Information

For this assay, SNP(s) [rs116381300] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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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