hi Ram - please see the link I have updated my post with. it contains a table I am working on from dbsnp. each snp id rsxxxxxxxxx appears to have an amino acid subsition (unless nonsense). So I am looking for the equivalent polyphen format of this table.
Hi - this is a very simple question. I am trying to use polyphen to score snps in batch. I have polyphen installed on my computer, and the input file it takes is in the following form:
P18887 399 R Q
P18074 751 K Q
P01023 1000 I V
Q9BUG6 186 L V
P15848 358 V M
Q9UNQ9 110 V I
P35568 158 P R
P06241 445 I F
P11245 286 G E
P12259 1764 V M
P51168 594 T M
P16581 575 L F
P08908 273 G D
Q92889 706 I T
Q92889 875 E G
O75360 142 A T
P11532 557 I T
P00451 1260 D E
which I'm sure is all familiar to you as the protein ID, position, ref amino acid and subsituted amino acid.
However, when looking on dbsnp if I search for any gene I might have expected a file in this format for a given gene. I am very surprised that this type of file is not readily available. Anyway I wondered how I can produce such a file? I am familiar with python/R and biopython/bioconductor. but SNPs is new to me.
For example I see a table like this: http://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?geneId=3603
where the table contains two of the needed fields - the substitued amino acid, and the position. but not the protein id or the reference amino acid.
Thank you.
1 answer
IMO dbSNP stores SNPs, which are nucleotide changes. You are looking for a specific type of nucleotide change - a non-synonymous SNP in a coding region (an SNP that causes an AA mutation).
I use PolyPhen to predict possible effects of mutations in proteins I analyze at my lab. This would mean that I have a protein sequence, and I know the mutation I'm looking for. (Like R399Q in P18887). Running this info through PolyPhen then becomes understandable.
If you're looking to run PolyPhen on all coding SNPs for a protein, you might wanna check out UniProt (or any such well-annotated protein resource) to get your list. Else, you're looking at a custom intermediate step to convert nucleotide variant information to AA mutation information before you can get to PolyPhen.
Hi, the contents of this table look like they're being computed on the fly, and are not available for download as a text file. You might wanna look for dbSNP remote querying features or use the genome browser.
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