Product Details

SNP ID

rs144796171

Assay Type

Functionally Tested

NCBI dbSNP Submissions

1

Location

Chr.6:30163747 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCCTGCCTGTACCCTCTGTGCGGG[A/G]CCGCTGGAGGATGCGGTGACCATTC

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	542	Intron			NP_006769.2
NM_052828.2	542	Intron			NP_439893.2
XM_011514221.1	542	Intron			XP_011512523.1
XM_011514222.2	542	Intron			XP_011512524.1
XM_011514223.2	542	Intron			XP_011512525.1
XM_011514225.1	542	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	542	Silent Mutation	GGA,GGG	G21G	NP_150232.2
XM_011514987.1	542	Intron			XP_011513289.1
XM_011514988.2	542	UTR 5			XP_011513290.1

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