Product Details

SNP ID
rs182681016
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:79201697 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATTTTTCATGACAATTCATTCTCC[C/T]TCGTTATCTACAGATTCAGTTTTCT
Phenotype
MIM: 604502
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
HMGN3 PubMed Links

Gene Details

Gene
HMGN3
Gene Name
high mobility group nucleosomal binding domain 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001201362.1 469 UTR 3 NP_001188291.1
NM_001201363.1 469 Silent Mutation GAA,GAG E128E NP_001188292.1
NM_001318884.1 469 UTR 3 NP_001305813.1
NM_001318885.1 469 Silent Mutation GAA,GAG E80E NP_001305814.1
NM_001318886.1 469 Silent Mutation GAA,GAG E126E NP_001305815.1
NM_001318887.1 469 UTR 3 NP_001305816.1
NM_001318888.1 469 Silent Mutation GAA,GAG E59E NP_001305817.1
NM_004242.3 469 Silent Mutation GAA,GAG E97E NP_004233.1
NM_138730.2 469 UTR 3 NP_620058.1

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