Product Details

SNP ID

rs7166434

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:45512915 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGCCGAGGTGGGAGAACTGCTTGAG[C/T]GTAAGAGTCTGAGGCTGCAGTAAGC

Phenotype

MIM: 611314 MIM: 602095

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

HMGN2P46 PubMed Links

Gene Details

Gene

HMGN2P46

Gene Name

high mobility group nucleosomal binding domain 2 pseudogene 46

There are no transcripts associated with this gene.

Gene

SLC30A4

Gene Name

solute carrier family 30 member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321036.1		Intron			NP_001307965.1
NM_013309.5		Intron			NP_037441.2
XM_011521997.2		Intron			XP_011520299.1
XM_017022560.1		Intron			XP_016878049.1
XM_017022561.1		Intron			XP_016878050.1
XM_017022562.1		Intron			XP_016878051.1

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