Product Details

SNP ID
rs140922673
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:42854368 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAATGCCACTTTGATCAGTTATTTG[C/T]TGTATGACTTCATTCAAAAACACTT
Phenotype
MIM: 614649
Polymorphism
C/T, Transition 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 2587 UTR 3 NP_001153695.1
NM_001160224.1 2587 Intron NP_001153696.1
NM_001160225.1 2587 UTR 3 NP_001153697.1
NM_030954.3 2587 UTR 3 NP_112216.3
XM_006716404.2 2587 UTR 3 XP_006716467.1
XM_006716405.2 2587 UTR 3 XP_006716468.1
XM_011544666.2 2587 UTR 3 XP_011542968.1
XM_017013881.1 2587 UTR 3 XP_016869370.1
XM_017013882.1 2587 UTR 3 XP_016869371.1

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