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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q8TAQ2: Variant p.Leu609Pro

SWI/SNF complex subunit SMARCC2
Gene: SMARCC2
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Variant information Variant position: help 609 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LP/P [Disclaimer] The variants are classified into three categories: LP/P, LB/B and US.
  • LP/P: likely pathogenic or pathogenic.
  • LB/B: likely benign or benign.
  • US: uncertain significance

Residue change: help From Leucine (L) to Proline (P) at position 609 (L609P, p.Leu609Pro). Indicates the amino acid change of the variant. The one-letter and three-letter codes for amino acids used in UniProtKB/Swiss-Prot are those adopted by the commission on Biochemical Nomenclature of the IUPAC-IUB.
Physico-chemical properties: help Similar physico-chemical property. Both residues are medium size and hydrophobic. The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -3 The score within a Blosum matrix for the corresponding wild-type to variant amino acid change. The log-odds score measures the logarithm for the ratio of the likelihood of two amino acids appearing by chance. The Blosum62 substitution matrix is used. This substitution matrix contains scores for all possible exchanges of one amino acid with another:
  • Lowest score: -4 (low probability of substitution).
  • Highest score: 11 (high probability of substitution).
More information can be found on the following page

Variant description: help In CSS8. Any additional useful information about the variant.


Sequence information Variant position: help 609 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 1214 The length of the canonical sequence.
Location on the sequence: help SKSKAAASATREWTEQETLL L LEALEMYKDDWNKVSEHVGS The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: help The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human                         SKSKAAASATREWTEQETLLLLEALEMYKDDWNKVSEHVGS

Mouse                         SKSKAAASATREWTEQETLLLLEALEMYKDDWNKVSEHVGS

Sequence annotation in neighborhood: help The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
  • Type: the type of sequence feature.
  • Positions: endpoints of the sequence feature.
  • Description: contains additional information about the feature.
TypePositionsDescription
Chain 1 – 1214 SWI/SNF complex subunit SMARCC2
Domain 596 – 647 SANT
Cross 592 – 592 Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO2)
Helix 603 – 615



Literature citations
Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay.
Machol K.; Rousseau J.; Ehresmann S.; Garcia T.; Nguyen T.T.M.; Spillmann R.C.; Sullivan J.A.; Shashi V.; Jiang Y.H.; Stong N.; Fiala E.; Willing M.; Pfundt R.; Kleefstra T.; Cho M.T.; McLaughlin H.; Rosello Piera M.; Orellana C.; Martinez F.; Caro-Llopis A.; Monfort S.; Roscioli T.; Nixon C.Y.; Buckley M.F.; Turner A.; Jones W.D.; van Hasselt P.M.; Hofstede F.C.; van Gassen K.L.I.; Brooks A.S.; van Slegtenhorst M.A.; Lachlan K.; Sebastian J.; Madan-Khetarpal S.; Sonal D.; Sakkubai N.; Thevenon J.; Faivre L.; Maurel A.; Petrovski S.; Krantz I.D.; Tarpinian J.M.; Rosenfeld J.A.; Lee B.H.; Campeau P.M.;
Am. J. Hum. Genet. 104:164-178(2019)
Cited for: INVOLVEMENT IN CSS8; VARIANTS CSS8 ASP-134; 241-TRP--GLN-1214 DEL; PRO-609; PRO-610; PRO-613; ARG-635; VAL-896 AND GLY-900;
Disclaimer: Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.