Product Details

SNP ID

rs138295689

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:45511241 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGCGCTTAGGTCAGTTAACATATG[A/C]AGTGCATCTGTCATGATTGCTAGGC

Phenotype

MIM: 611314 MIM: 602095

Polymorphism

A/C, Transversion 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	553	Silent Mutation	CTG,CTT	L145L	NP_001307965.1
NM_013309.5	553	Silent Mutation	CTG,CTT	L145L	NP_037441.2
XM_011521997.2	553	Silent Mutation	CTG,CTT	L145L	XP_011520299.1
XM_017022560.1	553	Silent Mutation	CTG,CTT	L145L	XP_016878049.1
XM_017022561.1	553	Silent Mutation	CTG,CTT	L145L	XP_016878050.1
XM_017022562.1	553	Silent Mutation	CTG,CTT	L145L	XP_016878051.1

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