Product Details

SNP ID
rs141133477
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:138773676 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGAAGGACAGGGGAAGCAATGAAA[C/T]GCCGAGGGCGGAGCCAAGAGCGACA
Phenotype
MIM: 615353
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CCDC28A PubMed Links

Gene Details

Gene
CCDC28A
Gene Name
coiled-coil domain containing 28A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015439.2 4 Missense Mutation ACG,ATG T1M NP_056254.1
XM_011535728.2 4 Missense Mutation ACG,ATG T1M XP_011534030.1
Gene
GVQW2
Gene Name
GVQW motif containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001242740.1 4 UTR 5 NP_001229669.1

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