Product Details

SNP ID

rs2390606

Assay Type

Functionally tested

NCBI dbSNP Submissions

42

Location

Chr.1:90712090 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CACCAGTCACACTGCTGTGGGGGAG[A/C]TTTCCAGCCCTGTTTCTAGGGGTGG

Phenotype

MIM: 605212

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

BARHL2 PubMed Links

Gene Details

Gene

BARHL2

Gene Name

BarH like homeobox 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020063.1	1428	UTR 3			NP_064447.1

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