Hello,
I downloaded the data_mutations_extended.txt file of both release 6.2 and 7.0,
I filtered the data according to the following values:
1. "Start_Position"(between 89618196 and 89733687),
2. "Chromosome"(10)
3. "Variant_Classification" (["Missense_Mutation", "Nonsense_Mutation", "Splice_Site", "Nonstop_Mutation", "Silent", "Splice_Region", "Translation_Start_Site"])
4. "Reference_Allele"== A or ==C or ==G or ==T and "Tumor_Seq_Allele2"== A or ==C or ==G or ==T.
According to these filters, I got **63 mutations in the 6.2 release data, and only 1 in the 7.0 release data**.
Is this kind of difference possible? I couldnt find a problem with my code to explain it otherwise.
Thank you!
Linoy
Created by linoy_tsaban Hello @linoy_tsaban,
Apologies for the delay in response. Unfortunately, I don't observe these 63 mutations, I only found 2 mutations that fit this criteria:
1. Chromosome: 10
1. Start_Position: 89720659
1. Reference_Allele: G
1. Tumor_Seq_Allele2: T
Is this what you mean by 89720659G>T? Other than that, the mutations counts can actually change from release to release due to corrections or updates in the data.
Best,
Tom
Thank you for yout reply!
In point 4 I ment I only kept samples whose "Reference_Allele" value and "Tumor_Seq_Allele2" value in ["A", "C","G","T"].
I know understand my question was not written well. After filtering the data acoording to the 4 steps I described, I got **63 mutations in position 89720659**, specifically: ****89720659G>T** appeared 63 times in release 6.2 but this same mutation only appeared once in release 7**.
Does it still make sense?
Thank you!! Hello @linoy_tsaban,
Im not certain I understand bullet point #4. If you look in the [data release page](https://www.synapse.org/#!Synapse:syn7222066/wiki/410924), it has brief descriptions of the patches made to the releases. It is entirely possible for variant data to change between releases due to sites retracting / revising data.
Best,
Tom
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