Shell Programming and Scripting

Chr    Position    Ref    Alt    Score    Gene    HGVS_C   HGVS_P    Coding_Consequence    dbSNP
1    17312743    C    T    1    Gene1    -    ATP13A2:NM_001141974.2:exon27:c.3214G>A:p.A1072T;ATP13A2:NM_001141973.2:exon29:c.3501G>A:p.P1167P,ATP13A2:NM_022089.3:exon29:c.3516G>A:p.P1172P    SNV    1
1    17313343    G    A    1    Gene2    -    ATP13A2:NM_001141973.2:exon27:c.3177C>T:p.A1059A,ATP13A2:NM_001141974.2:exon26:c.3060C>T:p.A1020A,ATP13A2:NM_022089.3:exon27:c.3192C>T:p.A1064A    SNV    2
1    17313654    C    T    1    Gene3    -    ATP13A2:NM_001141973.2:exon26:c.2955G>A:p.V985V,ATP13A2:NM_001141974.2:exon25:c.2838G>A:p.V946V,ATP13A2:NM_022089.3:exon26:c.2970G>A:p.V990Vsynonymous    SNV    3
1    17314942    G    A    1    Gene4    -    ATP13A2:NM_001141973.2:exon24:c.2622C>T:p.G874G,ATP13A2:NM_001141974.2:exon23:c.2505C>T:p.G835G,ATP13A2:NM_022089.3:exon24:c.2637C>T:p.G879Gsynonymous    SNV    4
1    17319011    G    A    1    Gene5    -    ATP13A2:NM_001141973.2:exon17:c.1800C>T:p.P600P,ATP13A2:NM_001141974.2:exon17:c.1800C>T:p.P600P,ATP13A2:NM_022089.3:exon17:c.1815C>T:p.P605Psynonymous    SNV    5
1    20960230    C    T    1    Gene6    -    PINK1:NM_032409.2:exon1:c.189C>T:p.L63L    SNV    6
1    20964328    A    G    1    Gene7    NM_032409.2:exon2:c.388-7A>G    -    -    7
1    20972048    G    A    1    Gene8    NM_032409.2:exon5:c.960-5G>A;NR_046507.1:exon2:c.3981+30C>T    -    -    8
 1    43395635    C    T    1    Gene9    -    SLC2A1:NM_006516.2:exon5:c.588G>A:p.P196P    synonymous    9

CHROM    POS    ID    REF    ALT    ANN[*].FEATUREID:ANN[*].HGVS_C    ANN[*].HGVS_P
1    17312743    rs3170740    C    T    NM_001141974.2:c.3214G>A,NM_022089.3:c.3516G>A,NM_001141973.2:c.3501G>A,NM_001135247.1:c.-7975G>A,NM_017459.2:c.-7975G>A    p.Ala1072Thr,p.Pro1172Pro,p.Pro1167Pro,.,.
1    17313343    rs9435659    G    A    NM_022089.3:c.3192C>T,NM_001141973.2:c.3177C>T,NM_001141974.2:c.3060C>T    p.Ala1064Ala,p.Ala1059Ala,p.Ala1020Ala
1    17313654    rs761421    C    T    NM_022089.3:c.2970G>A,NM_001141973.2:c.2955G>A,NM_001141974.2:c.2838G>A    p.Val990Val,p.Val985Val,p.Val946Val
1    17314942    rs9435662    G    A    NM_022089.3:c.2637C>T,NM_001141973.2:c.2622C>T,NM_001141974.2:c.2505C>T    p.Gly879Gly,p.Gly874Gly,p.Gly835Gly
1    17319011    rs2076603    G    A    NM_022089.3:c.1815C>T,NM_001141973.2:c.1800C>T,NM_001141974.2:c.1800C>T    p.Pro605Pro,p.Pro600Pro,p.Pro600Pro
1    20960230    rs45530340    C    T    NM_032409.2:c.189C>T,NR_106732.1:n.59C>T    p.Leu63Leu,.
1    20964328    rs2298298    A    G    NM_032409.2:c.388-7A>G,NR_106732.1:n.*4047A>G,NR_046507.1:n.*4822T>C    .,.,.
1    20972048    rs3131713    G    A    NM_032409.2:c.960-5G>A,NR_046507.1:n.3981+30C>T    .,.
1    43395635    rs2229682    C    T    NM_006516.2:c.588G>A    p.Pro196Pro

Chr    Position    Ref    Alt    Score    Gene    HGVS_C    HGVS_P    Coding_Consequence    dbSNP
1    17312743    C    T    1    Gene1    NM_001141974.2:c.3214G>A,NM_022089.3:c.3516G>A,NM_001141973.2:c.3501G>A,NM_001135247.1:c.-7975G>A,NM_017459.2:c.-7975G>A    p.Ala1072Thr,p.Pro1172Pro,p.Pro1167Pro,.,.    SNV    1
1    17313343    G    A    1    Gene2    NM_022089.3:c.3192C>T,NM_001141973.2:c.3177C>T,NM_001141974.2:c.3060C>T    p.Ala1064Ala,p.Ala1059Ala,p.Ala1020Ala    SNV    2
1    17313654    C    T    1    Gene3    NM_022089.3:c.2970G>A,NM_001141973.2:c.2955G>A,NM_001141974.2:c.2838G>A    p.Val990Val,p.Val985Val,p.Val946Val    SNV    3
1    17314942    G    A    1    Gene4    NM_022089.3:c.2637C>T,NM_001141973.2:c.2622C>T,NM_001141974.2:c.2505C>T    p.Gly879Gly,p.Gly874Gly,p.Gly835Gly    SNV    4
1    17319011    G    A    1    Gene5    NM_022089.3:c.1815C>T,NM_001141973.2:c.1800C>T,NM_001141974.2:c.1800C>T    p.Pro605Pro,p.Pro600Pro,p.Pro600Pro    SNV    5
1    20960230    C    T    1    Gene6    NM_032409.2:c.189C>T,NR_106732.1:n.59C>T    p.Leu63Leu    SNV    6
1    20964328    A    G    1    Gene7    NM_032409.2:c.388-7A>G,NR_106732.1:n.*4047A>G,NR_046507.1:n.*4822T>C    -    -    7
1    20972048    G    A    1    Gene8    NM_032409.2:c.960-5G>A,NR_046507.1:n.3981+30C>T    -    -    8
 1    43395635    C    T    1    Gene9    NM_006516.2:c.588G>A    p.Pro196Pro    synonymous    9

#replace column 6 from file 1 with column 7 from file 2

 awk 'FNR==NR{a[NR]=$6; next}{$7=a[FNR]}1' FS='\t' OFS='\t' file2 file1 > file3


#replace column 7 from file 1 with column 8 from file 2

 awk 'FNR==NR{a[NR]=$7; next}{$8=a[FNR]}1' FS='\t' OFS='\t' file2 file3 > file4


#remove pattern from column 7 from file
awk '{gsub(/\.,.*/,"-");}1' file4 > final.txt #patterns not changed with this command

awk '
FNR==1 {
   if (NR>1) print
   next
}
{ key = $1 FS $2 }
FNR==NR{
    hgvs_c[key]=$6
    hgvs_p[key]=$7
    next
}
key in hgvs_c {
   $7 = hgvs_c[key]
   $8 = hgvs_p[key]
}
{ gsub(/\t[\.,]{2,}[^\t]*/, "\t-") }
1' FS='\t' OFS='\t' file2 file1