Product Details

SNP ID

rs2523733

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:30163738 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCATGAGCTGCCTGCCTGTACCCT[A/C]TGTGCGGGGCCGCTGGAGGATGCGG

Phenotype

MIM: 605701

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

TRIM10 PubMed Links

Gene Details

Gene

TRIM10

Gene Name

tripartite motif containing 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006778.3	533	Intron			NP_006769.2
NM_052828.2	533	Intron			NP_439893.2
XM_011514221.1	533	Intron			XP_011512523.1
XM_011514222.2	533	Intron			XP_011512524.1
XM_011514223.2	533	Intron			XP_011512525.1
XM_011514225.1	533	Intron			XP_011512527.1

Gene

TRIM15

Gene Name

tripartite motif containing 15

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033229.2	533	Silent Mutation	CTA,CTC	L18L	NP_150232.2
XM_011514987.1	533	Intron			XP_011513289.1
XM_011514988.2	533	UTR 5			XP_011513290.1

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