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SNP ID

rs202238726

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:164957278 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGGAGAAGCGAATCGTTTTCTCC[C/G]CGTGCCCTGTCAGCCGCTCATGGTG

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FAM218A PubMed Links

Gene Details

Gene

FAM218A

Gene Name

family with sequence similarity 218 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_153027.1	331	Missense Mutation			NP_694572.1

Gene

TRIM61

Gene Name

tripartite motif containing 61

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012414.2	331	Intron			NP_001012414.1

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