Product Details

SNP ID
rs201117972
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:44147981 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACTGTGCAGGCACAGTCCTCCAGG[C/T]TGCTGCTGTTACACCCCACTGCTCC
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
C17orf53 PubMed Links

Gene Details

Gene
C17orf53
Gene Name
chromosome 17 open reading frame 53
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001171251.2 269 Silent Mutation CTG,TTG L60L NP_001164722.1
NM_001321310.1 269 Silent Mutation CTG,TTG L60L NP_001308239.1
NM_001321311.1 269 Silent Mutation CTG,TTG L60L NP_001308240.1
NM_024032.4 269 Silent Mutation CTG,TTG L60L NP_076937.2
XM_011525187.1 269 Silent Mutation CTG,TTG L60L XP_011523489.1
XM_011525188.1 269 Silent Mutation CTG,TTG L60L XP_011523490.1
XM_011525189.1 269 Silent Mutation CTG,TTG L60L XP_011523491.1
XM_011525190.1 269 Silent Mutation CTG,TTG L60L XP_011523492.1
XM_011525191.2 269 Silent Mutation CTG,TTG L60L XP_011523493.1
XM_011525192.1 269 Silent Mutation CTG,TTG L60L XP_011523494.1
XM_011525193.1 269 Silent Mutation CTG,TTG L60L XP_011523495.1
XM_011525194.1 269 Silent Mutation CTG,TTG L60L XP_011523496.1
XM_011525195.1 269 Silent Mutation CTG,TTG L60L XP_011523497.1
XM_011525197.2 269 Intron XP_011523499.1
XM_017025031.1 269 UTR 5 XP_016880520.1
XM_017025032.1 269 UTR 5 XP_016880521.1

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