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Hi,
I got whole genome annotated data from a company in excel format. The data is annotated with dbSNP135_full and dbSNP135_common. The variants which are not present in these two versions of dbSNP are actually novel variants.
Now we have our own data annotated with annovar but when I checked some SNPs which are not present in dbSNP135, they are there in dbSNP database. I think the version which is used by annovar is build 132. How can I add another version like build 137, so that if I want to look for only novel mutations, I may not face the problems?
I got whole genome annotated data from a company in excel format. The data is annotated with dbSNP135_full and dbSNP135_common. The variants which are not present in these two versions of dbSNP are actually novel variants.
Now we have our own data annotated with annovar but when I checked some SNPs which are not present in dbSNP135, they are there in dbSNP database. I think the version which is used by annovar is build 132. How can I add another version like build 137, so that if I want to look for only novel mutations, I may not face the problems?