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SNP ID

rs28647582

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:41747248 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCGGCCATGGGGCCCTAGGTCCTTC[C/T]CACTCGAGGCTCCAGGACTTCGAAT

Phenotype

MIM: 603851

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

PHOX2B PubMed Links

Gene Details

Gene

PHOX2B

Gene Name

paired like homeobox 2b

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003924.3		Intron			NP_003915.2

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