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I just noticed that ensembl has a variant table that might inspire us:
http://grch37.ensembl.org/Homo_sapiens/Gene/Variation_Gene/Table?db=core;g=ENSG00000136531;r=2:166095912-166248818
(inspiring one way or another) - one thing they have that we don't is the amino acid change.
I also wonder if we should provide links to clingen as well as exac. Example of the former:
http://www.ncbi.nlm.nih.gov/projects/dbvar/clingen/clingen_gene.cgi?sym=SCN2A
You can get to that via the NCBI link we provide so not critical
I'm not proposing sticking these in without more feedback
The text was updated successfully, but these errors were encountered:
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I just noticed that ensembl has a variant table that might inspire us:
http://grch37.ensembl.org/Homo_sapiens/Gene/Variation_Gene/Table?db=core;g=ENSG00000136531;r=2:166095912-166248818
(inspiring one way or another) - one thing they have that we don't is the amino acid change.
I also wonder if we should provide links to clingen as well as exac. Example of the former:
http://www.ncbi.nlm.nih.gov/projects/dbvar/clingen/clingen_gene.cgi?sym=SCN2A
You can get to that via the NCBI link we provide so not critical
I'm not proposing sticking these in without more feedback
The text was updated successfully, but these errors were encountered: