Product Details

SNP ID

rs2974617

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:115126658 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCATCTGATCCATATCATAGAAAT[C/T]TACTTTGCCTTTATCACAGTCAAGG

Phenotype

MIM: 609317

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TRIM36 PubMed Links

Gene Details

Gene

TRIM36

Gene Name

tripartite motif containing 36

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001017397.1	2553	Intron			NP_001017397.1
NM_001017398.1	2553	Intron			NP_001017398.1
NM_001300752.1	2553	Missense Mutation	AAT,GAT	N523D	NP_001287681.1
NM_001300759.1	2553	Missense Mutation	AAT,GAT	N666D	NP_001287688.1
NM_018700.3	2553	Missense Mutation	AAT,GAT	N678D	NP_061170.2
XM_017009621.1	2553	Missense Mutation	AAT,GAT	N695D	XP_016865110.1
XM_017009622.1	2553	Missense Mutation	AAT,GAT	N683D	XP_016865111.1
XM_017009623.1	2553	Intron			XP_016865112.1

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