Product Details

SNP ID

rs76170879

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:139231935 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAGTTCAGTTACCCGGAGCTGCTG[C/T]TGTGCGGAGAACAACGGGTACAGAA

Phenotype

MIM: 613841

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

UBN2 PubMed Links

Gene Details

Gene

UBN2

Gene Name

ubinuclein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173569.3	2371	Silent Mutation	CTG,TTG	L151L	NP_775840.3
XM_005250249.3	2371	Silent Mutation	CTG,TTG	L151L	XP_005250306.2
XM_006715916.3	2371	Silent Mutation	CTG,TTG	L151L	XP_006715979.2
XM_011516002.2	2371	Silent Mutation	CTG,TTG	L151L	XP_011514304.1
XM_011516003.1	2371	Silent Mutation	CTG,TTG	L151L	XP_011514305.1

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