Product Details

SNP ID

rs17194467

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:30163808 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACCTTCTGCCGGCTCTGCCTCCCC[A/G]CGCTCTCCCAGATGGGGGCCCAATC

Phenotype

MIM: 605701

Polymorphism

A/G, Transition 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	603	Intron			NP_006769.2
NM_052828.2	603	Intron			NP_439893.2
XM_011514221.1	603	Intron			XP_011512523.1
XM_011514222.2	603	Intron			XP_011512524.1
XM_011514223.2	603	Intron			XP_011512525.1
XM_011514225.1	603	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	603	Missense Mutation	ACG,GCG	T42A	NP_150232.2
XM_011514987.1	603	Intron			XP_011513289.1
XM_011514988.2	603	UTR 5			XP_011513290.1

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