Product Details

SNP ID
rs200120193
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.16:30782230 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGGGGCTGGGCCCTGCGCCTTCCC[C/G]TAGGCCAATTCTATAATCAGGAAAG
Phenotype
MIM: 607700
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
RNF40 PubMed Links

Gene Details

Gene
RNF40
Gene Name
ring finger protein 40
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001207033.1 2306 Intron NP_001193962.1
NM_001207034.1 2306 Intron NP_001193963.1
NM_001286572.2 2306 Intron NP_001273501.1
NM_014771.3 2306 Intron NP_055586.1
XM_011545997.1 2306 Intron XP_011544299.1
Gene
ZNF629
Gene Name
zinc finger protein 629
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001080417.1 2306 Missense Mutation CGG,GGG R700G NP_001073886.1
XM_005255222.3 2306 Missense Mutation CGG,GGG R686G XP_005255279.1

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