Product Details

SNP ID

rs3825016

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:64591814 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CGCCGGGCCCCAACCAGAGGCCCCA[C/T]CAGTGCCGCCGCTTCCGCCAGCCAC

Phenotype

MIM: 607096

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC22A12 PubMed Links

Gene Details

Gene

SLC22A12

Gene Name

solute carrier family 22 member 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001276326.1	1005	Silent Mutation	CAC,CAT	H86H	NP_001263255.1
NM_001276327.1	1005	Silent Mutation	CAC,CAT	H86H	NP_001263256.1
NM_144585.3	1005	Silent Mutation	CAC,CAT	H86H	NP_653186.2
NM_153378.2	1005	UTR 5			NP_700357.1
XM_006718430.3	1005	Silent Mutation	CAC,CAT	H86H	XP_006718493.1
XM_006718431.3	1005	Silent Mutation	CAC,CAT	H51H	XP_006718494.1

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