Product Details

SNP ID
rs145440300
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:159161291 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGATAACAGATGGCACAAATATCA[C/T]TGTGTTTCTCAAGCTGCTCTTTCGT
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 1814 Missense Mutation AAT,AGT N564S NP_001186309.1
NM_001199381.1 1814 Missense Mutation AAT,AGT N551S NP_001186310.1
NM_001199382.1 1814 Missense Mutation AAT,AGT N548S NP_001186311.1
NM_001199383.1 1814 Missense Mutation AAT,AGT N534S NP_001186312.1
NM_144726.2 1814 Missense Mutation AAT,AGT N562S NP_653327.1
XM_017009138.1 1814 Missense Mutation AAT,AGT N534S XP_016864627.1

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