Product Details

SNP ID
rs4799632
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.18:32100930 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGAGATATATTTAAATTAAAATAAA[C/T]GCTCAGAAAAATGGTGTAATTACAA
Phenotype
MIM: 616319
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
RNF138 PubMed Links

Gene Details

Gene
RNF138
Gene Name
ring finger protein 138
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001191324.1 Intron NP_001178253.2
NM_016271.4 Intron NP_057355.2
NM_198128.2 Intron NP_937761.1
XM_005258285.1 Intron XP_005258342.1
XM_005258286.1 Intron XP_005258343.1

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