Product Details

SNP ID
rs199724794
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:68261817 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGAGTTTTGTCTACCACGGCCTGG[G/T]TGAGGGGCTCAGTGGTGACCACCAT
Phenotype
MIM: 610880
Polymorphism
G/T, Transversion 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 1620 Intron NP_001287842.1
NM_022338.3 1620 Missense Mutation AAC,ACC N393T NP_071733.1
XM_005274053.3 1620 Missense Mutation AAC,ACC N393T XP_005274110.1
XM_011545103.2 1620 Missense Mutation AAC,ACC N361T XP_011543405.1

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