Product Details

SNP ID

rs10783409

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:50942580 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCAAAATCCTTAGTTTAAAATGCAA[A/G]GCTTGGCTGGGTGTAGTGGCTCATG

Phenotype

MIM: 600523

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

HIGD1C PubMed Links

Additional Information

For this assay, SNP(s) [rs111623388] are located under a probe 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

HIGD1C

Gene Name

HIG1 hypoxia inducible domain family member 1C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001109619.1		Intron			NP_001103089.1
XM_011538649.2		Intron			XP_011536951.1
XM_017019783.1		Intron			XP_016875272.1
XM_017019784.1		Intron			XP_016875273.1
XM_017019785.1		Intron			XP_016875274.1

Gene

SLC11A2

Gene Name

solute carrier family 11 member 2

There are no transcripts associated with this gene.

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