Product Details

SNP ID
rs200349356
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:159159005 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGACAGCCTGCATGGAAAAAATGAC[C/T]GCAAGGCGTGATCACAGCAGATTTC
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 1870 Missense Mutation AGT,GGT S583G NP_001186309.1
NM_001199381.1 1870 Missense Mutation AGT,GGT S570G NP_001186310.1
NM_001199382.1 1870 Missense Mutation AGT,GGT S567G NP_001186311.1
NM_001199383.1 1870 Missense Mutation AGT,GGT S553G NP_001186312.1
NM_144726.2 1870 Missense Mutation AGT,GGT S581G NP_653327.1
XM_017009138.1 1870 Missense Mutation AGT,GGT S553G XP_016864627.1

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