This is not a single species VCF. OP has done a multiple sequence alignment of sequences from an unknown number of species. I don't think we know if human sequences are involved.
Is there any script or tool to Map gene SNP positions to genome coordinates, for example
CHROM POS ID REF ALT
1 60 . A T
60 is snp position in genes not chr 1
Now I want to find position of A in chr1, mean genomic position, of variant position in chromosomes not with in gene
for example gene start at 10000 position of chr1 , than inplace of 60 come 10060 mean genomic position of this variant. Please have any idea about it?
1 answer
My job here is to answer the question as stated, which is useful to anyone else who stumbles across this. If the OP is actually asking a different question to the one stated, that's on them.
Exactly, and the past threads I have tried to tell OP that he has to explain the context of his question. It's just impossible to have OP write what he wants and what he has done in one post. Anyway, this is the last thread I put some effort in understanding this.
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Refer to this previous thread from misbahabas to get background information essential for this thread: Is it possible to annotate single genes by snpeff
that thread is not usefull for me
genomax wrote that for everybody else who tries to make sense of your question because you fail EVERY TIME to provide important context to your post.