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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot A5YKK6: Variant p.Arg535Cys

CCR4-NOT transcription complex subunit 1
Gene: CNOT1
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Variant information Variant position: help 535 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 Arginine (R) to Cysteine (C) at position 535 (R535C, p.Arg535Cys). 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 Change from large size and basic (R) to medium size and polar (C) 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 HPE12. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 535 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 2376 The length of the canonical sequence.
Location on the sequence: help PNSAIILHYAWHGQGQSPSI R QLIMHAMAEWYMRGEQYDQA 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                         PNSAIILHYAWHGQGQSPSIRQLIMHAMAEWYMRGEQYDQA

Mouse                         PNSAIILHYAWHGQGQSPSIRQLIMHAMAEWYMRGEQYDQA

Xenopus tropicalis            PNSAIILHYAWHGQGQSPSIRQLIMHAMAEWYMRGEQYDQA

Zebrafish                     PNSAIILHYAWHGQGQSPSIRQLIMHSMAEWYMRGEQYDQA

Caenorhabditis elegans        PNVTPVLNLVWNDTSLSKHMRQHVIYCLTSMHAA----DSS
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 – 2376 CCR4-NOT transcription complex subunit 1
Helix 532 – 541



Literature citations
A specific CNOT1 mutation results in a novel syndrome of pancreatic agenesis and holoprosencephaly through impaired pancreatic and neurological development.
De Franco E.; Watson R.A.; Weninger W.J.; Wong C.C.; Flanagan S.E.; Caswell R.; Green A.; Tudor C.; Lelliott C.J.; Geyer S.H.; Maurer-Gesek B.; Reissig L.F.; Lango Allen H.; Caliebe A.; Siebert R.; Holterhus P.M.; Deeb A.; Prin F.; Hilbrands R.; Heimberg H.; Ellard S.; Hattersley A.T.; Barroso I.;
Am. J. Hum. Genet. 104:985-989(2019)
Cited for: VARIANT HPE12 CYS-535; INVOLVEMENT IN HPE12; A CCR4-NOT transcription complex, subunit 1, CNOT1, variant associated with holoprosencephaly.
Kruszka P.; Berger S.I.; Weiss K.; Everson J.L.; Martinez A.F.; Hong S.; Anyane-Yeboa K.; Lipinski R.J.; Muenke M.;
Am. J. Hum. Genet. 104:990-993(2019)
Cited for: VARIANT HPE12 CYS-535; INVOLVEMENT IN HPE12;
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.