Product Details

SNP ID

rs1789514

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.18:36112691 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

AAATGGTATTTTGGCTGTGAATGAA[C/T]AGAAGTTTCCCAAACCAACTCTGTA

Phenotype

MIM: 608731

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC39A6 PubMed Links

Gene Details

Gene

SLC39A6

Gene Name

solute carrier family 39 member 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001099406.1		Intron			NP_001092876.1
NM_012319.3		Intron			NP_036451.3
XM_011525900.1		Intron			XP_011524202.1
XM_011525901.1		Intron			XP_011524203.1

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