Product Details

SNP ID
rs141067581
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:159158722 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATCTTTCGCACTGTGAGGATATTCT[C/T]TGGGGTCAAAAGCCCCTTCCTGGTT
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RNF145 PubMed Links

Gene Details

Gene
RNF145
Gene Name
ring finger protein 145
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199380.1 2153 Missense Mutation AAA,AGA K677R NP_001186309.1
NM_001199381.1 2153 Missense Mutation AAA,AGA K664R NP_001186310.1
NM_001199382.1 2153 Missense Mutation AAA,AGA K661R NP_001186311.1
NM_001199383.1 2153 Missense Mutation AAA,AGA K647R NP_001186312.1
NM_144726.2 2153 Missense Mutation AAA,AGA K675R NP_653327.1
XM_017009138.1 2153 Missense Mutation AAA,AGA K647R XP_016864627.1

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