SIFT predicts whether an amino acid substitution affects protein function based on sequence homology and the physical properties of amino acids. SIFT can be applied to naturally occurring nonsynonymous polymorphisms and laboratory-induced missense mutations.

LATEST UPDATES (Mar 2012) For all updates, please click on History tab.
Genome Tools Single Protein Tools
1.   genome coding variants filter tool Restrict to coding variants
BLink toolSIFT BLink
2a. SIFT missense / nonsynonymous SNV toolSIFT nonsynonymous single nucleotide variants (genome-scale)
protein sequence toolSIFT Sequence
2b. coding indels toolClassify coding indels (Insertion/Deletions)
New! Prediction on frameshifting indel
protein homologues toolSIFT Related Sequence
protein aligned sequences toolSIFT Aligned Sequences
Batch Tools
protein batch toolSIFT Batch Protein
Updated!
SIFT dbSNP toolSIFT dbSNP 132
SIFT for in-house use (version 4.0.5, released November, 2011)New!


Run SIFT on the Amazon Cloud New!


Copyright

Source code & executables (Sun, Linux)Download SIFT exe New! March 20/2012

SIFT database for SIFT version 5.0.0Download SIFT database New! March 20/2012

Please download the following database as well if you are using SIFT frameshifting indel tool
SIFT Coding Info database for SIFT version 5.0.0Download SIFT database New! March 20/2012

Report bugs

Prediction on human SNPsDownload SIFT pre-computed human SNPs data

Test sets for initial training of SIFT algorithm

Literature


Our review "Predicting the Effects of Amino Acid Substitutions on Protein Function" in Annual Review of Genomics and Human Genetics

Chapter

Supplementary Table 1



Referencing SIFT
Other Similar ToolsOther Similar Prediction Tools

This website is maintained by the group of Pauline Ng, creator of SIFT. Pauline developed and maintained the SIFT website
at Fred Hutchinson Cancer Researcher Center from 2001-2008, then the J. Craig Venter Institute from 2008-2010, and she is
now at the Genome Institute of Singapore.

Server support is provided by Georg Schneider, creator of protein function prediction tool ANNIE.

Recent changes to SIFT

March 2012
February 2012
  • SIFT nsSNVs tool updated to dbSNP 135
  • Fixed strand issues for some dbSNP rs ids
  • Reference allele predictions provided
January 2012
November 2011
  • SIFT tool for nsSNVs in genome now includes RefSeq, UCSC, and CCDS annotations in addition to Ensemble

June 2011
March 2011
  • Restrict coding tool now accepts the following formats: PileUp, VCF4.0, MAQ, SOAP, GFF3, CASAVA, cg as well as SIFT' own comma-delimited format.
  • Optimized SIFT Indel tool for speed.
  • SIFT Indel tool provides option to check presence in 1000 genome.
February 2011
  • Upgraded database to dbSNP build 132
  • Added HCB, JPT and YRI allele frequencies
  • Included presence in 1000 Genomes (1000 Genome July 2010 data release)
  • Fixed issues pertaining to inexact dbSNP matches. Previously, only checked coordinate positions. Now, also checking allele.
  • Fixed issues pertaining to wrong coordinates in Y chromosome, data regenerated from using information from UCSC.