Product Details

SNP ID
rs3845960
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:126527792 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCTTCAGGTACTGCTGGAGTGTCCC[A/G]AGTTCAGAGGACCTCCAGAAAGTAC
Phenotype
MIM: 610124
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C3orf22 PubMed Links

Gene Details

Gene
C3orf22
Gene Name
chromosome 3 open reading frame 22
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_152533.2 2246 Intron NP_689746.1
XM_011512455.2 2246 Intron XP_011510757.1
XM_011512457.2 2246 Intron XP_011510759.1
XM_017005751.1 2246 Intron XP_016861240.1
XM_017005752.1 2246 Intron XP_016861241.1
XM_017005753.1 2246 UTR 3 XP_016861242.1
Gene
CHST13
Gene Name
carbohydrate sulfotransferase 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_152889.2 2246 Intron NP_690849.1

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