Product Details

SNP ID

rs17194460

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:30163769 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGGCCGCTGGAGGATGCGGTGACC[A/G]TTCCCTGTGGACACACCTTCTGCCG

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	564	Intron			NP_006769.2
NM_052828.2	564	Intron			NP_439893.2
XM_011514221.1	564	Intron			XP_011512523.1
XM_011514222.2	564	Intron			XP_011512524.1
XM_011514223.2	564	Intron			XP_011512525.1
XM_011514225.1	564	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	564	Missense Mutation	ATT,GTT	I29V	NP_150232.2
XM_011514987.1	564	Intron			XP_011513289.1
XM_011514988.2	564	UTR 5			XP_011513290.1

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