Product Details

SNP ID

rs7782122

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:139233089 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTATGGTCAAAATGACTGACTGCTT[A/C]GTCACAAAGTATCATGTTGAACAAT

Phenotype

MIM: 613841

Polymorphism

A/C, Transversion 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		Intron			NP_775840.3
XM_005250249.3		Intron			XP_005250306.2
XM_006715916.3		Intron			XP_006715979.2
XM_011516002.2		Intron			XP_011514304.1
XM_011516003.1		Intron			XP_011514305.1

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