PolyPhen-2 prediction of functional effects of human nsSNPs

PolyPhen-2 (Polymorphism Phenotyping v2) is a tool which predicts possible impact of an amino acid substitution on the structure and function of a human protein using straightforward physical and comparative considerations. Please, use the form below to submit your query.

WHESS.db provides quick access to precomputed set of PolyPhen-2 predictions for whole human exome sequence space (WHESS). It contains annotations for all single-nucleotide non-synonymous (missense) codon changes enumerated at each CDS codon position in the exons of 43,043 UCSC knownGene transcripts (hg19/GRCh37) with maximum sequence overlap and identity to known UniProtKB proteins.

Query WHESS.db
Enter search:
Note:
Use genomic coordinates for GRCh37/hg19 with
allele nucleotides in plus strand orientation
Search Examples
P06241 445 I F
FYN_HUMAN 410 G R
NP_005792 59 L P
rs1801108
chr1:1267483 G/A
chr1:1158631 A/C,G,T