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Merge pull request #754 from griffithlab/proximal_dnp
Handle proximal DNP variants affecting multiple amino acids
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chromosome_name start stop reference variant gene_name transcript_name transcript_support_level amino_acid_change codon_change ensembl_gene_id hgvsc hgvsp wildtype_amino_acid_sequence frameshift_amino_acid_sequence fusion_amino_acid_sequence variant_type protein_position transcript_expression gene_expression normal_depth normal_vaf tdna_depth tdna_vaf trna_depth trna_vaf index protein_length_change | ||
chr16 28593449 28593450 AG GA SULT1A2 ENST00000335715 1 A/V gCT/gTC ENSG00000197165 ENST00000335715.9:c.491_492delinsTC ENSP00000338742.4:p.Ala164Val MELIQDISRPPLEYVKGVPLIKYFAEALGPLQSFQARPDDLLISTYPKSGTTWVSQILDMIYQGGDLEKCHRAPIFMRVPFLEFKVPGIPSGMETLKNTPAPRLLKTHLPLALLPQTLLDQKVKVVYVARNAKDVAVSYYHFYHMAKVYPHPGTWESFLEKFMAGEVSYGSWYQHVQEWWELSRTHPVLYLFYEDMKENPKREIQKILEFVGRSLPEETVDLMVEHTSFKEMKKNPMTNYTTVRREFMDHSISPFMRKGMAGDWKTTFTVAQNERFDADYAKKMAGCSLSFRSEL missense 164 NA 0.0534405615378929 NA NA 185 0.136 NA NA 1.SULT1A2.ENST00000335715.missense.164A/V | ||
chr16 28593449 28593450 AG GA SULT1A2 ENST00000395630 5 A/V gCT/gTC ENSG00000197165 ENST00000395630.5:c.491_492delinsTC ENSP00000378992.1:p.Ala164Val MELIQDISRPPLEYVKGVPLIKYFAEALGPLQSFQARPDDLLISTYPKSGTTWVSQILDMIYQGGDLEKCHRAPIFMRVPFLEFKVPGIPSGMETLKNTPAPRLLKTHLPLALLPQTLLDQKVKVVYVARNAKDVAVSYYHFYHMAKVYPHPGTWESFLEKFMAGEVSYGSWYQHVQEWWELSRTHPVLYLFYEDMKENPKREIQKILEFVGRSLPEETVDLMVEHTSFKEMKKNPMTNYTTVRREFMDHSISPFMRKGMAGDWKTTFTVAQNERFDADYAKKMAGCSLSFRSEL missense 164 NA 0.0534405615378929 NA NA 185 0.136 NA NA 2.SULT1A2.ENST00000395630.missense.164A/V | ||
chr16 28593449 28593450 AG GA SULT1A2 ENST00000526384 3 A/V gCT/gTC ENSG00000197165 ENST00000526384.1:c.491_492delinsTC ENSP00000435358.1:p.Ala164Val MELIQDISRPPLEYVKGVPLIKYFAEALGPLQSFQARPDDLLISTYPKSGTTWVSQILDMIYQGGDLEKCHRAPIFMRVPFLEFKVPGIPSGMETLKNTPAPRLLKTHLPLALLPQTLLDQKVKVVYVARNAKDVAVSYYHFYHMAKVYPHPGTWESFLEKFMAGEVSYGSWYQHVQEWWELSRTHPVLYLF missense 164 NA 0.0534405615378929 NA NA 185 0.136 NA NA 3.SULT1A2.ENST00000526384.missense.164A/V | ||
chr16 28593449 28593450 AG GA SULT1A2 ENST00000534108 2 GW/GR ggCTgg/ggTCgg ENSG00000197165 ENST00000534108.5:c.576_577delinsTC ENSP00000433075.1:p.Trp193Arg MELIQDISRPPLEYVKGVPLIKYFAEALGPLQSFQARPDDLLISTYPKSGTTWVSQILDMIYQGGDLEKCHRAPIFMRVPFLEFKVPGIPSGVCVLGARGVEEDRAGASAHQTFPDPLLRDGDSEKHTSPTTPEDTPAPGSAPPDSVGSEGQGGLCCPQRKGCGGFLLPLLPHGQSVPSPWDLGKLPGEVHGWRSVLWVLVPARARVVGAEPHPPCSLPLL missense 192-193 NA 0.0534405615378929 NA NA 185 0.136 NA NA 4.SULT1A2.ENST00000534108.missense.192-193GW/GR | ||
chr16 28593449 28593450 AG GA AC020765.6 ENST00000677940 NA A/V gCT/gTC ENSG00000288656 ENST00000677940.1:c.257_258delinsTC ENSP00000503077.1:p.Ala86Val MLAKLLCDQVVGAPIAVSAFYAGMSILQGKDDIFLDLKQKFWNTYMVVYVARNAKDVAVSYYHFYHMAKVYPHPGTWESFLEKFMAGEVSYGSWYQHVQEWWELSRTHPVLYLFYEDMKENPKREIQKILEFVGRSLPEETVDLMVEHTSFKEMKKNPMTNYTTVRREFMDHSISPFMRKGMAGDWKTTFTVAQNERFDADYAKKMAGC missense 86 NA 0.0 NA NA 185 0.136 NA NA 5.AC020765.6.ENST00000677940.missense.86A/V | ||
chr16 28593472 28593473 T G SULT1A2 ENST00000335715 1 E/D gaA/gaC ENSG00000197165 ENST00000335715.9:c.468A>C ENSP00000338742.4:p.Glu156Asp MELIQDISRPPLEYVKGVPLIKYFAEALGPLQSFQARPDDLLISTYPKSGTTWVSQILDMIYQGGDLEKCHRAPIFMRVPFLEFKVPGIPSGMETLKNTPAPRLLKTHLPLALLPQTLLDQKVKVVYVARNAKDVAVSYYHFYHMAKVYPHPGTWESFLEKFMAGEVSYGSWYQHVQEWWELSRTHPVLYLFYEDMKENPKREIQKILEFVGRSLPEETVDLMVEHTSFKEMKKNPMTNYTTVRREFMDHSISPFMRKGMAGDWKTTFTVAQNERFDADYAKKMAGCSLSFRSEL missense 156 NA 0.0534405615378929 NA NA 195 0.121 0 NA 6.SULT1A2.ENST00000335715.missense.156E/D | ||
chr16 28593472 28593473 T G SULT1A2 ENST00000395630 5 E/D gaA/gaC ENSG00000197165 ENST00000395630.5:c.468A>C ENSP00000378992.1:p.Glu156Asp MELIQDISRPPLEYVKGVPLIKYFAEALGPLQSFQARPDDLLISTYPKSGTTWVSQILDMIYQGGDLEKCHRAPIFMRVPFLEFKVPGIPSGMETLKNTPAPRLLKTHLPLALLPQTLLDQKVKVVYVARNAKDVAVSYYHFYHMAKVYPHPGTWESFLEKFMAGEVSYGSWYQHVQEWWELSRTHPVLYLFYEDMKENPKREIQKILEFVGRSLPEETVDLMVEHTSFKEMKKNPMTNYTTVRREFMDHSISPFMRKGMAGDWKTTFTVAQNERFDADYAKKMAGCSLSFRSEL missense 156 NA 0.0534405615378929 NA NA 195 0.121 0 NA 7.SULT1A2.ENST00000395630.missense.156E/D | ||
chr16 28593472 28593473 T G SULT1A2 ENST00000526384 3 E/D gaA/gaC ENSG00000197165 ENST00000526384.1:c.468A>C ENSP00000435358.1:p.Glu156Asp MELIQDISRPPLEYVKGVPLIKYFAEALGPLQSFQARPDDLLISTYPKSGTTWVSQILDMIYQGGDLEKCHRAPIFMRVPFLEFKVPGIPSGMETLKNTPAPRLLKTHLPLALLPQTLLDQKVKVVYVARNAKDVAVSYYHFYHMAKVYPHPGTWESFLEKFMAGEVSYGSWYQHVQEWWELSRTHPVLYLF missense 156 NA 0.0534405615378929 NA NA 195 0.121 0 NA 8.SULT1A2.ENST00000526384.missense.156E/D | ||
chr16 28593472 28593473 T G SULT1A2 ENST00000534108 2 K/Q Aag/Cag ENSG00000197165 ENST00000534108.5:c.553A>C ENSP00000433075.1:p.Lys185Gln MELIQDISRPPLEYVKGVPLIKYFAEALGPLQSFQARPDDLLISTYPKSGTTWVSQILDMIYQGGDLEKCHRAPIFMRVPFLEFKVPGIPSGVCVLGARGVEEDRAGASAHQTFPDPLLRDGDSEKHTSPTTPEDTPAPGSAPPDSVGSEGQGGLCCPQRKGCGGFLLPLLPHGQSVPSPWDLGKLPGEVHGWRSVLWVLVPARARVVGAEPHPPCSLPLL missense 185 NA 0.0534405615378929 NA NA 195 0.121 0 NA 9.SULT1A2.ENST00000534108.missense.185K/Q | ||
chr16 28593472 28593473 T G AC020765.6 ENST00000677940 NA E/D gaA/gaC ENSG00000288656 ENST00000677940.1:c.234A>C ENSP00000503077.1:p.Glu78Asp MLAKLLCDQVVGAPIAVSAFYAGMSILQGKDDIFLDLKQKFWNTYMVVYVARNAKDVAVSYYHFYHMAKVYPHPGTWESFLEKFMAGEVSYGSWYQHVQEWWELSRTHPVLYLFYEDMKENPKREIQKILEFVGRSLPEETVDLMVEHTSFKEMKKNPMTNYTTVRREFMDHSISPFMRKGMAGDWKTTFTVAQNERFDADYAKKMAGC missense 78 NA 0.0 NA NA 195 0.121 0 NA 10.AC020765.6.ENST00000677940.missense.78E/D |
16 changes: 16 additions & 0 deletions
16
tests/test_data/fasta_generator/proximal_dnp/output.cut_off.fasta
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>1 | ||
SFLEKFMAGEVSYGS | ||
>2 | ||
SFLEKFMVGEVSYGS | ||
>3 | ||
KLPGEVHGWRSVLWVL | ||
>4 | ||
QLPGEVHGRRSVLWVL | ||
>5 | ||
YPHPGTWESFLEKFM | ||
>6 | ||
YPHPGTWDSFLEKFM | ||
>7 | ||
PSPWDLGKLPGEVHG | ||
>8 | ||
PSPWDLGQLPGEVHG |
28 changes: 28 additions & 0 deletions
28
tests/test_data/fasta_generator/proximal_dnp/output.cut_off.key
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1: | ||
- WT.1.SULT1A2.ENST00000335715.missense.164A/V | ||
- WT.2.SULT1A2.ENST00000395630.missense.164A/V | ||
- WT.3.SULT1A2.ENST00000526384.missense.164A/V | ||
- WT.5.AC020765.6.ENST00000677940.missense.86A/V | ||
2: | ||
- MT.1.SULT1A2.ENST00000335715.missense.164A/V | ||
- MT.2.SULT1A2.ENST00000395630.missense.164A/V | ||
- MT.3.SULT1A2.ENST00000526384.missense.164A/V | ||
- MT.5.AC020765.6.ENST00000677940.missense.86A/V | ||
3: | ||
- WT.4.SULT1A2.ENST00000534108.missense.192-193GW/GR | ||
4: | ||
- MT.4.SULT1A2.ENST00000534108.missense.192-193GW/GR | ||
5: | ||
- WT.6.SULT1A2.ENST00000335715.missense.156E/D | ||
- WT.7.SULT1A2.ENST00000395630.missense.156E/D | ||
- WT.8.SULT1A2.ENST00000526384.missense.156E/D | ||
- WT.10.AC020765.6.ENST00000677940.missense.78E/D | ||
6: | ||
- MT.6.SULT1A2.ENST00000335715.missense.156E/D | ||
- MT.7.SULT1A2.ENST00000395630.missense.156E/D | ||
- MT.8.SULT1A2.ENST00000526384.missense.156E/D | ||
- MT.10.AC020765.6.ENST00000677940.missense.78E/D | ||
7: | ||
- WT.9.SULT1A2.ENST00000534108.missense.185K/Q | ||
8: | ||
- MT.9.SULT1A2.ENST00000534108.missense.185K/Q |
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Original file line number | Diff line number | Diff line change |
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@@ -0,0 +1,16 @@ | ||
>1 | ||
WESFLEKFMAGEVSYGSWY | ||
>2 | ||
WDSFLEKFMVGEVSYGSWY | ||
>3 | ||
LGKLPGEVHGWRSVLWVLVP | ||
>4 | ||
LGQLPGEVHGRRSVLWVLVP | ||
>5 | ||
KVYPHPGTWESFLEKFMAG | ||
>6 | ||
KVYPHPGTWDSFLEKFMVG | ||
>7 | ||
SVPSPWDLGKLPGEVHGWR | ||
>8 | ||
SVPSPWDLGQLPGEVHGRR |
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Original file line number | Diff line number | Diff line change |
---|---|---|
@@ -0,0 +1,28 @@ | ||
1: | ||
- WT.1.SULT1A2.ENST00000335715.missense.164A/V | ||
- WT.2.SULT1A2.ENST00000395630.missense.164A/V | ||
- WT.3.SULT1A2.ENST00000526384.missense.164A/V | ||
- WT.5.AC020765.6.ENST00000677940.missense.86A/V | ||
2: | ||
- MT.1.SULT1A2.ENST00000335715.missense.164A/V | ||
- MT.2.SULT1A2.ENST00000395630.missense.164A/V | ||
- MT.3.SULT1A2.ENST00000526384.missense.164A/V | ||
- MT.5.AC020765.6.ENST00000677940.missense.86A/V | ||
3: | ||
- WT.4.SULT1A2.ENST00000534108.missense.192-193GW/GR | ||
4: | ||
- MT.4.SULT1A2.ENST00000534108.missense.192-193GW/GR | ||
5: | ||
- WT.6.SULT1A2.ENST00000335715.missense.156E/D | ||
- WT.7.SULT1A2.ENST00000395630.missense.156E/D | ||
- WT.8.SULT1A2.ENST00000526384.missense.156E/D | ||
- WT.10.AC020765.6.ENST00000677940.missense.78E/D | ||
6: | ||
- MT.6.SULT1A2.ENST00000335715.missense.156E/D | ||
- MT.7.SULT1A2.ENST00000395630.missense.156E/D | ||
- MT.8.SULT1A2.ENST00000526384.missense.156E/D | ||
- MT.10.AC020765.6.ENST00000677940.missense.78E/D | ||
7: | ||
- WT.9.SULT1A2.ENST00000534108.missense.185K/Q | ||
8: | ||
- MT.9.SULT1A2.ENST00000534108.missense.185K/Q |
11 changes: 11 additions & 0 deletions
11
tests/test_data/fasta_generator/proximal_dnp/proximal_variants.tsv
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chromosome_name start stop reference variant amino_acid_change codon_change protein_position type main_somatic_variant | ||
chr16 28593472 28593473 T G E/D gaA/gaC 156 somatic 1.SULT1A2.ENST00000335715.missense.164A/V | ||
chr16 28593472 28593473 T G E/D gaA/gaC 156 somatic 2.SULT1A2.ENST00000395630.missense.164A/V | ||
chr16 28593472 28593473 T G E/D gaA/gaC 156 somatic 3.SULT1A2.ENST00000526384.missense.164A/V | ||
chr16 28593472 28593473 T G K/Q Aag/Cag 185 somatic 4.SULT1A2.ENST00000534108.missense.192-193GW/GR | ||
chr16 28593472 28593473 T G E/D gaA/gaC 78 somatic 5.AC020765.6.ENST00000677940.missense.86A/V | ||
chr16 28593449 28593450 AG GA A/V gCT/gTC 164 somatic 6.SULT1A2.ENST00000335715.missense.156E/D | ||
chr16 28593449 28593450 AG GA A/V gCT/gTC 164 somatic 7.SULT1A2.ENST00000395630.missense.156E/D | ||
chr16 28593449 28593450 AG GA A/V gCT/gTC 164 somatic 8.SULT1A2.ENST00000526384.missense.156E/D | ||
chr16 28593449 28593450 AG GA GW/GR ggCTgg/ggTCgg 192-193 somatic 9.SULT1A2.ENST00000534108.missense.185K/Q | ||
chr16 28593449 28593450 AG GA A/V gCT/gTC 86 somatic 10.AC020765.6.ENST00000677940.missense.78E/D |
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