Product Details

SNP ID
rs10372
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:19849775 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTTTCTTCCTACTTTCCAGGAAGGT[A/G]TTGTTTTGTTGTTTTCACAATTGTA
Phenotype
MIM: 610778
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C22orf29 PubMed Links

Gene Details

Gene
C22orf29
Gene Name
chromosome 22 open reading frame 29
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_024627.5 2998 UTR 3 NP_078903.3
Gene
GNB1L
Gene Name
G protein subunit beta 1 like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_053004.2 2998 Intron NP_443730.1

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