Hello,
I wanted to discuss frameshift mutations that difficult to interpret. I used both VCF file as well bam file to visualize them but I am unable to interpret what does bam or VCF telling me about that mutation.
e.g. in case of Bam file, IGV tells me that DEL 21 INS 6 G870(100%), T 0(0%)
Kindly can someone help me understanding such information? also if someone can explain the VCF information as well.
Thank you
e.g. this is the frameshift mutation at location chr7:151935798-151935799 GA>TG in gene KMT2C. now what is IGV telling me exactly?
Well, that is not a frameshift. As far as I can see from the image you have 2 adjacent SNPs, which is sometimes termed as Multiple Nucleotide Polymorphism (MNP). The first one occurs in position 98 in which a G is mutated to T, and the second one in position 99, in which an A is mutated to G. In the small window you have the number of total reads (depth) of the given position, 333, the number of reads containing an A, C, G, T and N for the given position.
Then what does DEL 7 means? because it a frameshift mutation at this position according to my data and am showing you that location with DEL 7
Sorry, I did not see that. Yes, there are 7 reads showing a deletion in that position. Although 45 reads say that there is a SNV there with a G.