Product Details

SNP ID

rs16837472

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:195579811 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTTTGCCAGTTTCAGAGACCATAGC[A/C]CTCAAGCTTCTCATCATCAGTATGT

Phenotype

MIM: 608733

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SLC39A10 PubMed Links

Gene Details

Gene

SLC39A10

Gene Name

solute carrier family 39 member 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001127257.1		Intron			NP_001120729.1
NM_020342.2		Intron			NP_065075.1
XM_005246689.4		Intron			XP_005246746.2
XM_011511504.2		Intron			XP_011509806.1
XM_011511505.2		Intron			XP_011509807.1
XM_011511506.2		Intron			XP_011509808.1
XM_011511507.2		Intron			XP_011509809.1
XM_017004522.1		Intron			XP_016860011.1
XM_017004523.1		Intron			XP_016860012.1

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