Product Details

SNP ID
rs139488436
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:36336677 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGATTCCAAAAAACACCCCTGTGAG[A/C]TTTCACAATCTGAAACGGCAAAATG
Phenotype
MIM: 612488
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
RNF38 PubMed Links

Gene Details

Gene
RNF38
Gene Name
ring finger protein 38
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_022781.4 4845 UTR 3 NP_073618.3
NM_194328.2 4845 UTR 3 NP_919309.1
NM_194329.2 4845 UTR 3 NP_919310.1
NM_194330.2 4845 UTR 3 NP_919311.1
NM_194332.2 4845 UTR 3 NP_919313.1
XM_005251366.3 4845 UTR 3 XP_005251423.1
XM_005251367.3 4845 UTR 3 XP_005251424.1
XM_005251368.3 4845 UTR 3 XP_005251425.1
XM_006716721.3 4845 UTR 3 XP_006716784.1
XM_011517712.2 4845 UTR 3 XP_011516014.1
XM_011517713.2 4845 UTR 3 XP_011516015.1
XM_017014294.1 4845 UTR 3 XP_016869783.1
XM_017014295.1 4845 UTR 3 XP_016869784.1
XM_017014296.1 4845 UTR 3 XP_016869785.1
XM_017014297.1 4845 UTR 3 XP_016869786.1

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