Product Details

SNP ID

rs2444007

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.15:44754927 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ATCCACCAACCCCTCCTCCAACATC[A/G]ATCCAGGCGACTATGTTGAAATGAA

Phenotype

MIM: 616017

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TRIM69 PubMed Links

Gene Details

Gene

TRIM69

Gene Name

tripartite motif containing 69

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001301144.1	377	Intron			NP_001288073.1
NM_001301145.1	377	Intron			NP_001288074.1
NM_001301146.1	377	Intron			NP_001288075.1
NM_080745.4	377	Intron			NP_542783.2
NM_182985.4	377	Missense Mutation	AAT,GAT	N12D	NP_892030.3

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