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SNP ID

rs115172371

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:42012646 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTATTTGGTAATGTCTTAATTTCT[C/T]TTTAATTTTTGAAGGATAGTTTTGC

Phenotype

MIM: 610981

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

WBP2NL PubMed Links

Gene Details

Gene

WBP2NL

Gene Name

WBP2 N-terminal like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152613.2		Intron			NP_689826.2

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