Product Details

SNP ID
rs202139930
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:42856225 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAGAGATGTAGATAAGCAATAAAAA[C/G]ATGACAAAGAAATCATCTAGAAAGC
Phenotype
MIM: 614649
Polymorphism
C/G, 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_001160223.1 730 Missense Mutation ATC,ATG I237M NP_001153695.1
NM_001160224.1 730 Intron NP_001153696.1
NM_001160225.1 730 Missense Mutation ATC,ATG I153M NP_001153697.1
NM_030954.3 730 Missense Mutation ATC,ATG I237M NP_112216.3
XM_006716404.2 730 Missense Mutation ATC,ATG I237M XP_006716467.1
XM_006716405.2 730 Missense Mutation ATC,ATG I187M XP_006716468.1
XM_011544666.2 730 Missense Mutation ATC,ATG I237M XP_011542968.1
XM_017013881.1 730 Missense Mutation ATC,ATG I237M XP_016869370.1
XM_017013882.1 730 Missense Mutation ATC,ATG I153M XP_016869371.1

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