Product Details

SNP ID

rs139859

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.22:37945127 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TTTTCCGTTCCTCCATGTCCTTCCC[C/T]GTGGCAAAGATATTTTGGAGTCTTT

Phenotype

MIM: 604414

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C22orf23 PubMed Links

Additional Information

For this assay, SNP(s) [rs35562630] are located under a primer 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

C22orf23

Gene Name

chromosome 22 open reading frame 23

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001207062.1	449	Silent Mutation			NP_001193991.1
NM_032561.4	449	Silent Mutation			NP_115950.3
XM_005261781.1	449	Silent Mutation			XP_005261838.1
XM_005261782.3	449	Silent Mutation			XP_005261839.1
XM_005261783.2	449	Silent Mutation			XP_005261840.1
XM_005261784.2	449	Silent Mutation			XP_005261841.1

Gene

MICALL1

Gene Name

MICAL like 1

There are no transcripts associated with this gene.

Gene

POLR2F

Gene Name

RNA polymerase II subunit F

There are no transcripts associated with this gene.

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