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Add Phenotype OMIM number to vcf file

Hi,

How can I annotate or compare the variants I have got in my vcf file that include the gene name to known mutations in the same gene but different chr location for instance from OMIM? For example I have searched manually on OMIM for MED25 gene, this is the output:

Gene-Phenotype Relationships Location Phenotype Phenotype MIM number Inheritance Phenotype mapping key 19q13.33 ?Charcot-Marie-Tooth disease, type 2B2 605589 AR 3 Basel-Vanagait-Smirin-Yosef syndrome 616449 AR 3

And my file is a multi vcf :

chr19   50321587        rs114843375;138201      A       G       6630.07 PASS    AC=10;A_F=0.052;AN=192;BaseQRankSum=1.74;ClippingRankSum=0.069;DP=4747;FS=1.147;GQ_MEAN=141.68;GQ_STDDEV=124.09;InbreedingCoeff=0.1560;MLEAC=10;MLEA_F=0.052;MQ=57.41;MQ0=0;MQRankSum=0.789;NCC=0;POSITIVE_TRAIN_SITE;QD=15.07;ReadPosRankSum=0.548;SOR=0.593;VQSLOD=5.04;culprit=MQ;EFF=UTR_5_PRIME(MODIFIER||12||MED25|protein_coding|CODING|NM_030973.3|1);AF=4.645e-03;COMMON=1;AF_ESP=0.0112;AF_EXAC=0.00869;AF_TGP=0.0102;ALLELEID=141904;CLNDISDB=MedGen:CN169374;CLNDN=not_specified;CLNHGVS=NC_000019.9:g.50321587A>G;CLNREVSTAT=criteria_provided,_single_submitter;CLNSIG=Benign;CLNVC=single_nucleotide_variant;CLNVCSO=SO:0001483;GENEINFO=MED25:81857;MC=SO:0001623|5_prime_UTR_variant;ORIGIN=1;RS=114843375        GT:AD:DP:GQ:PL  0/0:42,0:42:99:0,103,1320       0/0:48,0:48:99:0,120,1800

The output I want is to add the Phenotype MIM number in the end of the row:

chr19   50321587        rs114843375;138201      A       G       6630.07 PASS    AC=10;A_F=0.052;AN=192;BaseQRankSum=1.74;ClippingRankSum=0.069;DP=4747;FS=1.147;GQ_MEAN=141.68;GQ_STDDEV=124.09;InbreedingCoeff=0.1560;MLEAC=10;MLEA_F=0.052;MQ=57.41;MQ0=0;MQRankSum=0.789;NCC=0;POSITIVE_TRAIN_SITE;QD=15.07;ReadPosRankSum=0.548;SOR=0.593;VQSLOD=5.04;culprit=MQ;EFF=UTR_5_PRIME(MODIFIER||12||MED25|protein_coding|CODING|NM_030973.3|1);AF=4.645e-03;COMMON=1;AF_ESP=0.0112;AF_EXAC=0.00869;AF_TGP=0.0102;ALLELEID=141904;CLNDISDB=MedGen:CN169374;CLNDN=not_specified;CLNHGVS=NC_000019.9:g.50321587A>G;CLNREVSTAT=criteria_provided,_single_submitter;CLNSIG=Benign;CLNVC=single_nucleotide_variant;CLNVCSO=SO:0001483;GENEINFO=MED25:81857;MC=SO:0001623|5_prime_UTR_variant;ORIGIN=1;RS=114843375        GT:AD:DP:GQ:PL  0/0:42,0:42:99:0,103,1320       0/0:48,0:48:99:0,120,1800  605589, 616449

How can I approach this?

Thank you,

Pola

gene sequencing
• 2,757 views • link
written by psmirin • psmirin

Hi @Pierre Lindenbaum,

I have generated a file through http://www.ensembl.org/biomart (like you suggested)

The file is :

19      49818279        49838816        MED25   610197  605589

19      49818279        49838816        MED25   610197  616449

My file:

chr19   50338843        rs193291405;220933      C       G       PASS    1       4.401e-03       0.602   MedGen:CN043576|MedGen:CN169374 Charcot-Marie-Tooth_disease,_type_2|not_specified       NC_000019.9:g.50338843C>G        Benign/Likely_benign    single_nucleotide_variant       1       MODERATE        MED25   NM_030973.3     protein_coding  NON_SYNONYMOUS_CODING   MISSENSE        gCc/gGc A576G   CODING  4.66    B9TX30,B5ME50,Q71SY5     N       D,D,D,D,T,D,D,D B,B,B   N       5.71    B,B,B   .       0/0     0/0      55,0    38,0

I wanted to get this output:

chr19   50338843        rs193291405;220933      C       G       PASS    1       4.401e-03       0.602   MedGen:CN043576|MedGen:CN169374 Charcot-Marie-Tooth_disease,_type_2|not_specified       NC_000019.9:g.50338843C>G        Benign/Likely_benign    single_nucleotide_variant       1       MODERATE        MED25   NM_030973.3     protein_coding  NON_SYNONYMOUS_CODING   MISSENSE        gCc/gGc A576G   CODING  4.66    B9TX30,B5ME50,Q71SY5     N       D,D,D,D,T,D,D,D B,B,B   N       5.71    B,B,B   .       0/0     0/0      55,0    38,0    **610197:605589:616449**

I have tried to run the following command:

    awk 'NR==FNR{a[$4]=$5":"$6;next}{print $0,"\t",a[$17]}' FS="\t" med25omim med25test

This is the output that I get:

chr19   50338843        rs193291405;220933      C       G       PASS    1       4.401e-03       0.602   MedGen:CN043576|MedGen:CN169374 Charcot-Marie-Tooth_disease,_type_2|not_specified       NC_000019.9:g.50338843C>G        Benign/Likely_benign    single_nucleotide_variant       1       MODERATE        MED25   NM_030973.3     protein_coding  NON_SYNONYMOUS_CODING   MISSENSE        gCc/gGc A576G   CODING  4.66    B9TX30,B5ME50,Q71SY5     N       D,D,D,D,T,D,D,D B,B,B   N       5.71    B,B,B   .       0/0     0/0      55,0    38,0     **610197:616449**

I am missing this omimID 605589 Can you please help me to overcome this? Thank you very much, Pola

• 0 views • link
updated by Pierre Lindenbaum Pierre Lindenbaum • written by psmirin • psmirin

1 answer

use biomart http://www.ensembl.org/biomart/martview/ to build a BED file containing

chrom, start,end, mim_gene_accession

remove the lines without "mim_gene_accession", substract '1' to the start column to switch to a 0-based reference, sort on chrom/start, compress with bgzip and index with tabix. Something like:

$ awk '/^Gene/ {next;} {if($4!="") printf("%s\t%d\t%s\t%s\n",$3,int($1)-1,$2,$4);}' biomart.txt | sort -t $'\t' -k1,1 -k2,2n | bgzip > omim.bed.gz
$ tabix -f -p bed omim.bed.gz

then use something like http://lindenb.github.io/jvarkit/VCFBed.html to transfer the information into the VCF:

java -jar dist/vcfbed.jar -B omim.bed.gz -f '${4}' -T OMIM_ACN your.vcf
• 0 views • link
written by Pierre Lindenbaum Pierre Lindenbaum

Hi @Pierre Lindenbaum,

I have generated a file through http://www.ensembl.org/biomart (like you suggested)

The file is :

19      49818279        49838816        MED25   610197  605589

19      49818279        49838816        MED25   610197  616449

My file:

chr19   50338843        rs193291405;220933      C       G       PASS    1       4.401e-03       0.602   MedGen:CN043576|MedGen:CN169374 Charcot-Marie-Tooth_disease,_type_2|not_specified       NC_000019.9:g.50338843C>G        Benign/Likely_benign    single_nucleotide_variant       1       MODERATE        MED25   NM_030973.3     protein_coding  NON_SYNONYMOUS_CODING   MISSENSE        gCc/gGc A576G   CODING  4.66    B9TX30,B5ME50,Q71SY5     N       D,D,D,D,T,D,D,D B,B,B   N       5.71    B,B,B   .       0/0     0/0      55,0    38,0

I wanted to get this output:

chr19   50338843        rs193291405;220933      C       G       PASS    1       4.401e-03       0.602   MedGen:CN043576|MedGen:CN169374 Charcot-Marie-Tooth_disease,_type_2|not_specified       NC_000019.9:g.50338843C>G        Benign/Likely_benign    single_nucleotide_variant       1       MODERATE        MED25   NM_030973.3     protein_coding  NON_SYNONYMOUS_CODING   MISSENSE        gCc/gGc A576G   CODING  4.66    B9TX30,B5ME50,Q71SY5     N       D,D,D,D,T,D,D,D B,B,B   N       5.71    B,B,B   .       0/0     0/0      55,0    38,0    **610197:605589:616449**

I have tried to run the following command:

    awk 'NR==FNR{a[$4]=$5":"$6;next}{print $0,"\t",a[$17]}' FS="\t" med25omim med25test

This is the output that I get:

chr19   50338843        rs193291405;220933      C       G       PASS    1       4.401e-03       0.602   MedGen:CN043576|MedGen:CN169374 Charcot-Marie-Tooth_disease,_type_2|not_specified       NC_000019.9:g.50338843C>G        Benign/Likely_benign    single_nucleotide_variant       1       MODERATE        MED25   NM_030973.3     protein_coding  NON_SYNONYMOUS_CODING   MISSENSE        gCc/gGc A576G   CODING  4.66    B9TX30,B5ME50,Q71SY5     N       D,D,D,D,T,D,D,D B,B,B   N       5.71    B,B,B   .       0/0     0/0      55,0    38,0     **610197:616449**

I am missing this omimID 605589 Can you please help me to overcome this? Thank you very much, Pola

• 0 views • link
written by psmirin • psmirin

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