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SNP ID

rs4150229

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:140336318 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAAAAAGCAAGGGAGGACTTGAAG[C/G]CCTCAGCTAGATATGTTCCACGTGT

Phenotype

MIM: 126150

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

HBEGF PubMed Links

Gene Details

Gene

HBEGF

Gene Name

heparin binding EGF like growth factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001945.2		Intron			NP_001936.1

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