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SNP ID

rs6009675

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:49417491 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCCAGCTCTACCCAAAATACAGCA[C/G]CAAAGGTGATGGGCACTGCAGGCAG

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

C22orf34 PubMed Links

Gene Details

Gene

C22orf34

Gene Name

chromosome 22 open reading frame 34

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001289922.2		Intron			NP_001276851.1

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