#
# EASE-MM Genome: prediction of mutation-induced stability changes for the human genome
#
# This file describes the input format for the EASE-MM Genome web-server.
# If the line starts with '#' (hash), the line is ignored.
# The input format is compatible with the Variant Call Format (VCF): http://samtools.github.io/hts-specs/VCFv4.2.pdf
# EASE-MM requires only the first five VCF columns: CHR POS SEQ REF ALT.
# CHR: chromosome number (1-23XY)
# POS: 1-based position on the forward strand
# ID: this fiels is ignored by EASE-MM
# REF: reference nucleotide base
# ALT: mutated nucleotide base
# The server can predict only missense mutations in the GRCh37/hg19 assembly of the human genome.

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# Please note that the input size is limited to 10,000 variants per submission #
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# Examples #
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14 105643085 . G A
14 105685542 . C T
1 151536388 . G C
14 105716945 . C T
14 105944826 . A G
14 105995292 . G A
15 22853770 . C T
15 22855088 . G A
15 22866927 . T C
1 861324 . G A
1 861324 . G C