Product Details

SNP ID
rs200505706
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:68261877 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGGGTGCTGGGCTGGCACGAGTCC[A/G]TGGCTGGCATCTTAGTGCCCCCTGA
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 1560 Intron NP_001287842.1
NM_022338.3 1560 Missense Mutation ACG,ATG T373M NP_071733.1
XM_005274053.3 1560 Missense Mutation ACG,ATG T373M XP_005274110.1
XM_011545103.2 1560 Missense Mutation ACG,ATG T341M XP_011543405.1

View Full Product Details