Product Details

SNP ID

rs17011854

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:32168520 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTGAAGTTACTAAAATTACAAAGCA[A/G]TGTAACAAGTTGAAGGCTTTACTTT

Phenotype

MIM: 611148

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC30A6 PubMed Links

Gene Details

Gene

SLC30A6

Gene Name

solute carrier family 30 member 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_006712048.3		Intron			XP_006712111.1
XM_011532959.2		Intron			XP_011531261.1
XM_011532960.2		Intron			XP_011531262.1
XM_011532961.2		Intron			XP_011531263.1
XM_011532962.2		Intron			XP_011531264.1
XM_011532963.2		Intron			XP_011531265.1
XM_017004462.1		Intron			XP_016859951.1
XM_017004463.1		Intron			XP_016859952.1
XM_017004464.1		Intron			XP_016859953.1
XM_017004465.1		Intron			XP_016859954.1
XM_017004466.1		Intron			XP_016859955.1

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