Product Details

SNP ID

rs116715073

Assay Type

Functionally tested

NCBI dbSNP Submissions

9

Location

Chr.1:90712537 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAGGCTTGGGTGATAGAAATAAGG[C/T]GATGGAAACATCCTCTGCAGCGCCG

Phenotype

MIM: 605212

Polymorphism

C/T, Transition 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	981	Silent Mutation	TCA,TCG	S313S	NP_064447.1

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