Product Details

SNP ID
rs199981604
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:54330977 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGCTGCCTGGTGCCGTAGAGGCCCA[C/T]GGAGGAAAAGGAAGATAAGCATCAG
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
C2orf73 PubMed Links

Gene Details

Gene
C2orf73
Gene Name
chromosome 2 open reading frame 73
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001100396.1 114 Missense Mutation ACG,ATG T1M NP_001093866.1
XM_005264133.1 114 UTR 5 XP_005264190.1
XM_005264134.3 114 Intron XP_005264191.1
XM_011532510.2 114 Missense Mutation ACG,ATG T1M XP_011530812.1
XM_011532513.2 114 Intron XP_011530815.1
XM_017003323.1 114 Missense Mutation ACG,ATG T1M XP_016858812.1
XM_017003324.1 114 Missense Mutation ACG,ATG T1M XP_016858813.1

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