Product Details

SNP ID

rs199988558

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:35663699 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTATTGCCAGGAAGATAGGCAGCT[C/T]ATCTGTGTCCTGTGTCCAGTCATTG

Phenotype

MIM: 612298

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TRIM44 PubMed Links

Gene Details

Gene

TRIM44

Gene Name

tripartite motif containing 44

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017583.5	948	Silent Mutation	CTC,CTT	L196L	NP_060053.2
XM_006718254.1	948	Silent Mutation	CTC,CTT	L196L	XP_006718317.1

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