Product Details

SNP ID
rs10972861
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:36337469 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGAGAGAAGAAAAAGCTGCTACTC[C/T]TAGTCATTAGTACAATGTGCTGTGT
Phenotype
MIM: 612488
Polymorphism
C/T, Transition 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 4053 UTR 3 NP_073618.3
NM_194328.2 4053 UTR 3 NP_919309.1
NM_194329.2 4053 UTR 3 NP_919310.1
NM_194330.2 4053 UTR 3 NP_919311.1
NM_194332.2 4053 UTR 3 NP_919313.1
XM_005251366.3 4053 UTR 3 XP_005251423.1
XM_005251367.3 4053 UTR 3 XP_005251424.1
XM_005251368.3 4053 UTR 3 XP_005251425.1
XM_006716721.3 4053 UTR 3 XP_006716784.1
XM_011517712.2 4053 UTR 3 XP_011516014.1
XM_011517713.2 4053 UTR 3 XP_011516015.1
XM_017014294.1 4053 UTR 3 XP_016869783.1
XM_017014295.1 4053 UTR 3 XP_016869784.1
XM_017014296.1 4053 UTR 3 XP_016869785.1
XM_017014297.1 4053 UTR 3 XP_016869786.1

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