Product Details

SNP ID

rs1693532

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:58993820 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTGTGTTTTCCTGAGGGCATACAC[A/G]ATTAGCATCTTAGTTTAGTTTGTAT

Phenotype

MIM: 605840

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

RNF111 PubMed Links

Additional Information

For this assay, SNP(s) [rs79740936] 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

RNF111

Gene Name

ring finger protein 111

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001270528.1		Intron			NP_001257457.1
NM_001270529.1		Intron			NP_001257458.1
NM_001270530.1		Intron			NP_001257459.1
NM_017610.7		Intron			NP_060080.6
XM_005254479.3		Intron			XP_005254536.1
XM_006720575.3		Intron			XP_006720638.1
XM_006720579.3		Intron			XP_006720642.1
XM_011521694.2		Intron			XP_011519996.2
XM_011521696.2		Intron			XP_011519998.2
XM_011521697.2		Intron			XP_011519999.2
XM_011521699.2		Intron			XP_011520001.2
XM_017022336.1		Intron			XP_016877825.1
XM_017022337.1		Intron			XP_016877826.1
XM_017022338.1		Intron			XP_016877827.1
XM_017022339.1		Intron			XP_016877828.1
XM_017022340.1		Intron			XP_016877829.1
XM_017022341.1		Intron			XP_016877830.1
XM_017022342.1		Intron			XP_016877831.1
XM_017022343.1		Intron			XP_016877832.1

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