Product Details

SNP ID
rs3739351
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.8:42854443 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTATGAAAGGGAAGTTGGTGTCCTG[A/C]GTTCCTCACAAAATTATCCAAAGGA
Phenotype
MIM: 614649
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
RNF170 PubMed Links

Gene Details

Gene
RNF170
Gene Name
ring finger protein 170
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001160223.1 2512 UTR 3 NP_001153695.1
NM_001160224.1 2512 Intron NP_001153696.1
NM_001160225.1 2512 UTR 3 NP_001153697.1
NM_030954.3 2512 UTR 3 NP_112216.3
XM_006716404.2 2512 UTR 3 XP_006716467.1
XM_006716405.2 2512 UTR 3 XP_006716468.1
XM_011544666.2 2512 UTR 3 XP_011542968.1
XM_017013881.1 2512 UTR 3 XP_016869370.1
XM_017013882.1 2512 UTR 3 XP_016869371.1

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