Product Details

SNP ID

rs149864098

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:41219398 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGAGGAAAGTTTGGCACCCATGGC[A/G]TGGCGGTGCCCCAGGATGGGCAGGG

Phenotype

MIM: 109135

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

AXL PubMed Links

Additional Information

For this assay, SNP(s) [rs10411012] 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

AXL

Gene Name

AXL receptor tyrosine kinase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001278599.1	200	Intron			NP_001265528.1
NM_001699.5	200	Silent Mutation	GCA,GCG	A2A	NP_001690.2
NM_021913.4	200	Silent Mutation	GCA,GCG	A2A	NP_068713.2

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