Variant: rs869320694 

    present in Gene: FGFR1
    present in Chromosome: 8
    Position on Chromosome: 38414790
    Alleles of this Variant: T/C

rs869320694 in FGFR1 gene and Acute lymphoblastic leukemia with lymphomatous features PMID 26619011 2016 Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.

rs869320694 in FGFR1 gene and Astrocytoma PMID 26619011 2016 Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.

rs869320694 in FGFR1 gene and Encephalocraniocutaneous lipomatosis PMID 19224897 2009 The precise sequence of FGF receptor autophosphorylation is kinetically driven and is disrupted by oncogenic mutations.

PMID 26942290 2016 Using exome sequencing of DNA from multiple affected tissues from five unrelated individuals with ECCL, we identified two mosaic mutations, c.1638C>A (p.Asn546Lys) and c.1966A>G (p.Lys656Glu) within the tyrosine kinase domain of FGFR1, in two affected individuals each.

rs869320694 in FGFR1 gene and Glioblastoma PMID 26619011 2016 Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.

rs869320694 in FGFR1 gene and Liver carcinoma PMID 26619011 2016 Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.

rs869320694 in FGFR1 gene and Medulloblastoma PMID 26619011 2016 Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.

rs869320694 in FGFR1 gene and Transitional cell carcinoma of bladder PMID 26619011 2016 Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.