D641N (p.Asp641Asn) variant of FGFR1 (P11362)
D641N (p.Asp641Asn) in FGFR1 (P11362) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as pathogenic in the context of Hartsfield-Bixler-Demyer syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.72 / 1. The record also includes published literature and structural context.
D641N (p.Asp641Asn) variant details
- p.Asp641Asn
- rs1554548253
- ClinGen CA370730316
- cosmic curated COSV10966
- ClinVar RCV000614143
- Pathogenic
- Hartsfield-Bixler-Demyer syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.716
- AlphaMissense 1.00
- MetaLR 0.60
- MetaSVM 0.31
- PolyPhen-2 1.00
- SIFT 0.00
- EVE 0.92
- ClinVar: Pathogenic (Hartsfield-Bixler-Demyer syndrome)
- EBI: Pathogenic
- UniProt: Pathogenic
- Structural context available
- Cited in: Holoprosencephaly Overview. (PMID 20301702)
- Cited in: FGFR1-Related Hartsfield Syndrome. (PMID 26937548)