Product Details

SNP ID

rs149037758

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:75875009 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGCACCTGCTCACAATGGGTGAAG[C/T]GGGTGGGCGACAAGGGGTAGTTGAT

Phenotype

MIM: 611041

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TRIM47 PubMed Links

Gene Details

Gene

TRIM47

Gene Name

tripartite motif containing 47

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033452.2	1418	Missense Mutation	CAC,CGC	H464R	NP_258411.2
XM_005257787.4	1418	Missense Mutation	CAC,CGC	H226R	XP_005257844.1
XM_005257788.4	1418	Missense Mutation	CAC,CGC	H226R	XP_005257845.1

Gene

TRIM65

Gene Name

tripartite motif containing 65

There are no transcripts associated with this gene.

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