Hi everyone,
this is probably a minor issue, but for some SNVs I get different allele frequencies in the GnomAD column, depending whether I view the data in patient view, or whether I download the patient view as tsv.
For instance, this patient (
https://www.cbioportal.org/patient?sampleId=60&studyId=summit_2018) has a MITF2 T110M mutation. According to the data in patient view, this mutation occurs with an allele frequency of 0.00016 in populations. When I download the tsv it shows a frequency of
0.00018081293486300976. The difference is minor, but it doesn't seem to be a rounding issue, since I'd expect a 0.00018 in patient view instead.
Do you know the reason for the discrepancy? Is the GnomAD data assessed differently when downloading a .tsv file than in patient view?
Best wishes,
Thomas Pauli