Product Details

SNP ID
rs149411346
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:45522120 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGACTGTTGGTCAAAGGTAAGTCTT[G/T]GTCCAGTAAGGAATCATCGTCGGCC
Phenotype
MIM: 611314 MIM: 602095
Polymorphism
G/T, 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_001321036.1 353 Missense Mutation AAA,CAA K79Q NP_001307965.1
NM_013309.5 353 Missense Mutation AAA,CAA K79Q NP_037441.2
XM_011521997.2 353 Missense Mutation AAA,CAA K79Q XP_011520299.1
XM_017022560.1 353 Missense Mutation AAA,CAA K79Q XP_016878049.1
XM_017022561.1 353 Missense Mutation AAA,CAA K79Q XP_016878050.1
XM_017022562.1 353 Missense Mutation AAA,CAA K79Q XP_016878051.1

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