Product Details

SNP ID

rs73996007

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:75277224 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCCACATGCTTAGGGATCTCAAGG[A/G]ATGGACGCAGGTGAAGGGGCCATGG

Phenotype

MIM: 612072 MIM: 606521

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

LOC100287042 PubMed Links

Additional Information

For this assay, SNP(s) [rs192824470] 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

LOC100287042

Gene Name

uncharacterized LOC100287042

There are no transcripts associated with this gene.

Gene

MIF4GD

Gene Name

MIF4G domain containing

There are no transcripts associated with this gene.

Gene

SLC25A19

Gene Name

solute carrier family 25 member 19

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001126121.1		Intron			NP_001119593.1
NM_001126122.1		Intron			NP_001119594.1
NM_021734.4		Intron			NP_068380.3
XM_005257559.3		Intron			XP_005257616.1
XM_005257560.2		Intron			XP_005257617.1
XM_005257561.3		Intron			XP_005257618.1
XM_005257562.2		Intron			XP_005257619.1
XM_006722007.2		Intron			XP_006722070.1
XM_011525098.1		Intron			XP_011523400.1
XM_017024926.1		Intron			XP_016880415.1
XM_017024927.1		Intron			XP_016880416.1
XM_017024928.1		Intron			XP_016880417.1

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