Product Details

SNP ID
rs139139360
Assay Type
Functionally Tested
NCBI dbSNP Submissions
9
Location
Chr.21:39345211 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTTTAGTTTCTTGGTTAGCCACTT[C/T]GGCCTGTTTTCCCTTTGCTCCCCTT
Phenotype
MIM: 163920
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
HMGN1 PubMed Links

Gene Details

Gene
HMGN1
Gene Name
high mobility group nucleosome binding domain 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004965.6 387 Intron NP_004956.5
XM_011529543.1 387 Intron XP_011527845.1
XM_011529544.1 387 Intron XP_011527846.1
XM_011529545.1 387 Intron XP_011527847.1
XM_011529547.1 387 Intron XP_011527849.1
XM_011529549.1 387 Intron XP_011527851.1
XM_017028332.1 387 Intron XP_016883821.1
XM_017028333.1 387 Intron XP_016883822.1
XM_017028334.1 387 Intron XP_016883823.1
XM_017028335.1 387 Intron XP_016883824.1
XM_017028336.1 387 Intron XP_016883825.1
XM_017028338.1 387 Missense Mutation AAA,GAA K64E XP_016883827.1

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