Product Details

SNP ID
rs1042552
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:24285276 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACAAGCGACTGGGGCTGTCCGGACT[C/G]ACCCTCGCCCTGTCCCTGCTCGTGT
Phenotype
MIM: 162640
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
LOC107986777 PubMed Links

Gene Details

Gene
LOC107986777
Gene Name
uncharacterized LOC107986777
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_017012910.1 124 Intron XP_016868399.1
XM_017012911.1 124 Intron XP_016868400.1
Gene
NPY
Gene Name
neuropeptide Y
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000905.3 124 Silent Mutation CTC,CTG L12L NP_000896.1

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