Product Details

SNP ID

rs61751210

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.21:39345173 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTCAGTCTTCGTTTCCCCGTTTTC[C/T]GCAGGTAAGTCTTCTTTAGTTTCTT

Phenotype

MIM: 163920

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

HMGN1 PubMed Links

Additional Information

For this assay, SNP(s) [rs538463330] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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	425	Intron			NP_004956.5
XM_011529543.1	425	Intron			XP_011527845.1
XM_011529544.1	425	Intron			XP_011527846.1
XM_011529545.1	425	Intron			XP_011527847.1
XM_011529547.1	425	Intron			XP_011527849.1
XM_011529549.1	425	Intron			XP_011527851.1
XM_017028332.1	425	Intron			XP_016883821.1
XM_017028333.1	425	Intron			XP_016883822.1
XM_017028334.1	425	Intron			XP_016883823.1
XM_017028335.1	425	Intron			XP_016883824.1
XM_017028336.1	425	Intron			XP_016883825.1
XM_017028338.1	425	Silent Mutation	GCA,GCG	A76A	XP_016883827.1

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