Product Details

SNP ID

rs111334655

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:3573794 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGCGGGCGAGAAGGGGTCCCACGA[A/G]GAGGAGGTGAGAGTCCCTGCGCTGA

Phenotype

MIM: 605535

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

HMG20B PubMed Links

Gene Details

Gene

HMG20B

Gene Name

high mobility group 20B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006339.2	209	Silent Mutation	GAA,GAG	E47E	NP_006330.2
XM_017026144.1	209	Silent Mutation	GAA,GAG	E47E	XP_016881633.1

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