Product Details

SNP ID

rs77068590

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:110426203 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGACATTCCAAAGGAATTTTAAAGA[C/T]GTTTTCTGGTCTCTCAAGACACGGC

Phenotype

MIM: 608276

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC22A16 PubMed Links

Gene Details

Gene

SLC22A16

Gene Name

solute carrier family 22 member 16

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033125.3		Intron			NP_149116.2
XM_005267184.3		Intron			XP_005267241.1
XM_011536204.2		Intron			XP_011534506.1
XM_011536205.2		Intron			XP_011534507.1
XM_011536206.2		Intron			XP_011534508.1
XM_011536207.2		Intron			XP_011534509.1
XM_011536208.2		Intron			XP_011534510.1
XM_011536209.2		Intron			XP_011534511.1
XM_011536210.1		Intron			XP_011534512.1
XM_011536211.2		Intron			XP_011534513.1
XM_011536212.2		Intron			XP_011534514.1

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