Product Details

SNP ID

rs1804976

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:15160053 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGGAGGAGGCTCCCAACACTCCCC[A/C]GACCCCTGGCCCCAGTGGGTGCGCC

Phenotype

MIM: 600276

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

NOTCH3 PubMed Links

Additional Information

For this assay, SNP(s) [rs77669983] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

NOTCH3

Gene Name

notch 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000435.2	7434	UTR 3			NP_000426.2
XM_005259924.4	7434	UTR 3			XP_005259981.1

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