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SNP ID: rs12274893
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:5625803 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GTGCTACCAGCGTCTTCACCTGTCT[C/T]AGAACTTGCTCCTCATCATTCTTCC
Phenotype: MIM: 605684 MIM: 608487
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: TRIM34 PubMed Links

Gene Details

Gene: TRIM34
Gene Name: tripartite motif containing 34

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001003827.1		Intron			NP_001003827.1
NM_021616.5		Intron			NP_067629.2
NM_130390.2		Intron			NP_569074.2

Gene: TRIM5
Gene Name: tripartite motif containing 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033034.2		Intron			NP_149023.2
NM_033092.2		Intron			NP_149083.2
NM_033093.2		Intron			NP_149084.2
XM_005253183.2		Intron			XP_005253240.1
XM_005253184.2		Intron			XP_005253241.1
XM_006718358.2		Intron			XP_006718421.1
XM_011520426.2		Intron			XP_011518728.1
XM_011520427.1		Intron			XP_011518729.1
XM_017018460.1		Intron			XP_016873949.1
XM_017018461.1		Intron			XP_016873950.1
XM_017018462.1		Intron			XP_016873951.1
XM_017018463.1		Intron			XP_016873952.1

Gene: TRIM6-TRIM34
Gene Name: TRIM6-TRIM34 readthrough

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001003819.3		Intron			NP_001003819.1

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