Product Details

SNP ID

rs3009184

Assay Type

Validated

NCBI dbSNP Submissions

46

Location

Chr.1:119837385 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CTGTAAACAAATTCAGAAGAGCAGG[A/T]CATATTATGCAAATCACGCTTCACA

Phenotype

MIM: 613997

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

NBPF7 PubMed Links

Gene Details

Gene

NBPF7

Gene Name

neuroblastoma breakpoint family member 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001047980.2		Intron			NP_001041445.1
XM_017001186.1		Intron			XP_016856675.1

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