Product Details

SNP ID

hCV26876353

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:49031738 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTGCTCTGAATGCACAAAGTCAAC[A/C]GGGCAGATAAACCTCAAAACCAACA

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

TRIM49B PubMed Links

Gene Details

Gene

TRIM49B

Gene Name

tripartite motif containing 49B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001206626.1		Intron			NP_001193555.1

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