Product Details

SNP ID

rs3775532

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:75482210 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAAGAACTAGAAATGAACTGCACGC[A/G]TAGTGTCACTTAAAGCAAAGCTTCA

Phenotype

MIM: 607680

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

RCHY1 PubMed Links

Additional Information

For this assay, SNP(s) [rs9189] 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

RCHY1

Gene Name

ring finger and CHY zinc finger domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001009922.2	1111	UTR 3			NP_001009922.1
NM_001278536.1	1111	UTR 3			NP_001265465.1
NM_001278537.1	1111	UTR 3			NP_001265466.1
NM_001278538.1	1111	UTR 3			NP_001265467.1
NM_001278539.1	1111	UTR 3			NP_001265468.1
NM_015436.3	1111	UTR 3			NP_056251.2
XM_011531838.2	1111	UTR 3			XP_011530140.1
XM_011531839.2	1111	UTR 3			XP_011530141.1

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