Product Details

SNP ID
rs145151603
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:114126087 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAAGTGTGCCTGATTCTTCTCGTAA[A/C]ATATAACTTTGAATTATTCTGCAAA
Phenotype
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
CCDC186 PubMed Links

Gene Details

Gene
CCDC186
Gene Name
coiled-coil domain containing 186
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001321829.1 2022 Missense Mutation ATG,ATT M804I NP_001308758.1
NM_018017.3 2022 Missense Mutation ATG,ATT M804I NP_060487.2
NM_153249.1 2022 Intron NP_694981.1
XM_011539915.2 2022 Missense Mutation ATG,ATT M557I XP_011538217.1
XM_011539916.2 2022 Intron XP_011538218.1

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