Product Details

SNP ID
rs142071484
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:181195194 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGCCAGATTCGCAAGTAGGTGCCC[A/G]TGGAGCAAACAGAGAAAAGCGGGAA
Phenotype
MIM: 609315
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
LOC102577426 PubMed Links

Gene Details

Gene
LOC102577426
Gene Name
uncharacterized LOC102577426
There are no transcripts associated with this gene.

Gene
TRIM7
Gene Name
tripartite motif containing 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_033342.3 1582 Intron NP_203128.1
NM_203293.2 1582 Missense Mutation ACG,ATG T503M NP_976038.1
NM_203294.1 1582 Missense Mutation ACG,ATG T295M NP_976039.1
NM_203295.1 1582 Missense Mutation ACG,ATG T295M NP_976040.1
NM_203296.1 1582 Missense Mutation ACG,ATG T295M NP_976041.1
NM_203297.1 1582 Missense Mutation ACG,ATG T321M NP_976042.1
XM_017009903.1 1582 Missense Mutation ACG,ATG T295M XP_016865392.1
XM_017009904.1 1582 Intron XP_016865393.1

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