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Project description
Python pakcage for genomic variant analysis
variant-effect
command can infer the effect of a mutation
The input file has 5 columns: chromosome
, position
, strand
, reference allele
, alternative allele
.
- No header is required.
- The 3rd column (strand) is not used by default, just for compatibility with RNA mode.
- By default, the base of reference and alternative allele are based on DNA information
- For RNA mode (through
--rna
argument), the base of reference and alternative allele is reverse complement if the strand is negative(-).
eg:
Store the following table in sites.tsv.
chr3 10301112 - G T
chr7 94669540 + G N
chr2 215361150 - A T
chr15 72199549 - G T
chr17 81843580 - C T
chr2 84906537 + C T
chr14 23645352 + G T
chr20 37241351 + G T
chrX 153651037 + G T
chr17 81844010 - A T
By command: variant-effect -i sites.tsv -r human --rna
, the output will be:
#chrom pos strand ref alt mut_type gene_name transcript_id transcript_pos transcript_motif coding_pos codon_ref aa_pos aa_ref
chr3 10301112 - C A Silent SEC13 ENST00000397117 1441 TTGATCATCTGCCTTAACGTG 849 CTG 284 L
chr7 94669540 + G N ThreePrimeUTR PEG10 ENST00000612941 6240 TTTTACCCCTGTCAGTAGCCC None None None None
chr2 215361150 - T A ThreePrimeUTR FN1 ENST00000323926 8012 GGCCCGCAATACTGTAGGAAC None None None None
chr15 72199549 - C A ThreePrimeUTR PKM ENST00000319622 2197 GCTGTAACGTGGCACTGGTAG None None None None
chr17 81843580 - G A ThreePrimeUTR P4HB ENST00000681020 3061 AGAAGCTTGTCCCCCGTGTGG None None None None
chr2 84906537 + C T ThreePrimeUTR TMSB10 ENST00000233143 327 CCTGGGCACTCCGCGCCGATG None None None None
chr14 23645352 + G T ThreePrimeUTR DHRS2 ENST00000344777 1391 CTGCCATTCTGCCAGACTAGC None None None None
chr20 37241351 + G T ThreePrimeUTR RPN2 ENST00000237530 1959 AAAACTGAATGTCAAGAAAAG None None None None
chrX 153651037 + G T ThreePrimeUTR DUSP9 ENST00000342782 2145 CTGCTACTTTGGGGGGTGGGG None None None None
chr17 81844010 - T A ThreePrimeUTR P4HB ENST00000681020 2631 GAACTGTAATACGCAAAGCCA None None None None
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