Product Details

SNP ID
rs187513564
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:68261964 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTGGCTTCAGTCTCTACCTGCTCC[A/G]GTGCCTGGGATGTGCCTGGCCCAGC
Phenotype
MIM: 610880
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C11orf24 PubMed Links

Gene Details

Gene
C11orf24
Gene Name
chromosome 11 open reading frame 24
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001300913.1 1473 Intron NP_001287842.1
NM_022338.3 1473 Missense Mutation NP_071733.1
XM_005274053.3 1473 Missense Mutation XP_005274110.1
XM_011545103.2 1473 Missense Mutation XP_011543405.1

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