Product Details

SNP ID
rs202182023
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:181195575 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTGTTGGTGTCGAAGCGGCAGGGG[G/T]GGTTGGGCAGGTCCTGGGCCCGCTC
Phenotype
MIM: 609315
Polymorphism
G/T, Transversion 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 1201 Intron NP_203128.1
NM_203293.2 1201 Missense Mutation CAC,CCC H376P NP_976038.1
NM_203294.1 1201 Missense Mutation CAC,CCC H168P NP_976039.1
NM_203295.1 1201 Missense Mutation CAC,CCC H168P NP_976040.1
NM_203296.1 1201 Missense Mutation CAC,CCC H168P NP_976041.1
NM_203297.1 1201 Missense Mutation CAC,CCC H194P NP_976042.1
XM_017009903.1 1201 Missense Mutation CAC,CCC H168P XP_016865392.1
XM_017009904.1 1201 Intron XP_016865393.1

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