S20N (p.Ser20Asn) variant of TGFB2 (P61812)
S20N (p.Ser20Asn) in TGFB2 (P61812) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Loeys-Dietz syndrome 4. The record also includes published literature and structural context.
S20N (p.Ser20Asn) variant details
- p.Ser20Asn
- rs1656695125
- ClinGen CA344725186
- ClinVar RCV001824402
- gnomAD rs1656695125
- Uncertain significance
- Loeys-Dietz syndrome 4
- Missense
- ClinVar: Uncertain significance (Loeys-Dietz syndrome 4)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: Loeys-Dietz Syndrome. (PMID 20301312)