Product Details

SNP ID

rs11189493

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:98150975 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTTCCGGTGTAGTGATTGTGAGTC[G/T]GGGGGAAATTTTCTGCATTCTTGGT

Phenotype

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

R3HCC1L PubMed Links

Additional Information

For this assay, SNP(s) [rs118065643] 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

R3HCC1L

Gene Name

R3H domain and coiled-coil containing 1 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256619.1		Intron			NP_001243548.1
NM_001256620.1		Intron			NP_001243549.1
NM_001256621.1		Intron			NP_001243550.1
NM_014472.4		Intron			NP_055287.4
NM_138469.2		Intron			NP_612478.2
XM_011539639.1		Intron			XP_011537941.1
XM_011539640.1		Intron			XP_011537942.1
XM_011539641.1		Intron			XP_011537943.1
XM_011539642.1		Intron			XP_011537944.1
XM_011539643.1		Intron			XP_011537945.1
XM_011539644.1		Intron			XP_011537946.1
XM_011539645.2		Intron			XP_011537947.1
XM_011539646.1		Intron			XP_011537948.1
XM_011539647.1		Intron			XP_011537949.1
XM_011539648.1		Intron			XP_011537950.1
XM_011539649.1		Intron			XP_011537951.1
XM_017016074.1		Intron			XP_016871563.1
XM_017016075.1		Intron			XP_016871564.1
XM_017016076.1		Intron			XP_016871565.1
XM_017016077.1		Intron			XP_016871566.1
XM_017016078.1		Intron			XP_016871567.1
XM_017016079.1		Intron			XP_016871568.1
XM_017016080.1		Intron			XP_016871569.1
XM_017016081.1		Intron			XP_016871570.1
XM_017016082.1		Intron			XP_016871571.1
XM_017016083.1		Intron			XP_016871572.1

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