Product Details

SNP ID
rs200453165
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:41316625 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGAGCATGAGAAAGTGGCCATCCT[G/T]GCCCAGCTGTACCACGAGAAGCCAC
Phenotype
MIM: 605800
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
CCDC97 PubMed Links

Gene Details

Gene
CCDC97
Gene Name
coiled-coil domain containing 97
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_052848.1 410 Silent Mutation CTG,CTT L96L NP_443080.1
XM_005259377.4 410 Silent Mutation CTG,CTT L31L XP_005259434.1
XM_017027442.1 410 Silent Mutation CTG,CTT L150L XP_016882931.1
Gene
HNRNPUL1
Gene Name
heterogeneous nuclear ribonucleoprotein U like 1
There are no transcripts associated with this gene.

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