Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • help with polyphen output

    I have a list of variants and want to know if the variants are predicted to be deleterious or benign. When I did that using Polyphen2 and uploaded my variants as batch query, I got multiple possibilities for the prediction. For example, for the variant chr11:47306106 G/A, below is the Polyphen output, which one to pick? And what does this mean

    o_snp_id o_acc o_pos o_aa1 o_aa2 snp_id nt1 nt2 prediction
    chr11:47306106.GA.uc001ner.1 Q8WXG6 716 G E chr11:47306106.GA.uc001ner.1 G A possibly damaging
    chr11:47306106.GA.uc001nes.1 Q8WXG6-4 716 G E chr11:47306106.GA.uc001nes.1 G A benign
    chr11:47306106.GA.uc001net.1 Q8WXG6-2 716 G E chr11:47306106.GA.uc001net.1 G A benign
    chr11:47306106.GA.uc001neu.1 Q8WXG6-5 716 G E chr11:47306106.GA.uc001neu.1 G A possibly damaging
    chr11:47306106.GA.uc001nev.1 Q8WXG6-6 716 G E chr11:47306106.GA.uc001nev.1 G A benign
    chr11:47306106.GA.uc001new.2 Q8WXG6-3 716 G E chr11:47306106.GA.uc001new.2 G A possibly damaging
    chr11:47306106.GA.uc001nex.2 Q8WXG6-7 716 G E chr11:47306106.GA.uc001nex.2 G A possibly damaging
    chr11:47306106.GA.uc001nez.2 Q8WXG6-5 716 G E chr11:47306106.GA.uc001nez.2 G A possibly damaging
    chr11:47306106.GA.uc009yln.1 B5MEE5 716 G E chr11:47306106.GA.uc009yln.1 G A benign

    acc pos aa1 aa2 nt1 nt2 prediction
    Q8WXG6 716 G E G A possibly damaging
    Q8WXG6-4 716 G E G A benign
    Q8WXG6-2 716 G E G A benign
    Q8WXG6-5 716 G E G A possibly damaging
    Q8WXG6-6 716 G E G A benign
    Q8WXG6-3 716 G E G A possibly damaging
    Q8WXG6-7 716 G E G A possibly damaging
    Q8WXG6-5 716 G E G A possibly damaging
    B5MEE5 716 G E G A benign

  • #2
    The protein encoded by this gene (MADD) has 8 different isoforms and the position of your variant happens to overlap with all of them. Hence you got predictions for all sequences, which may differ, and do differ slightly in your case. You may decide to go with the prediction outcome for "canonical" isoform (Q8WXG6), or select more suitable isoform based on your knowledge of specifics of the biology of the process you study, or even try to "average" all predictions for all isoforms. There were 2 "benign" and 3 "possible damaging" predictions, the latter being not a strong effect indicator, hence overall, your variant is more probable to be benign.

    The last isoform (B5MEE5) comes from an unvalidated EMBL transcript and can be ignored.

    For details, see:


    Comment

    Latest Articles

    Collapse

    • seqadmin
      Essential Discoveries and Tools in Epitranscriptomics
      by seqadmin




      The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
      04-22-2024, 07:01 AM
    • seqadmin
      Current Approaches to Protein Sequencing
      by seqadmin


      Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
      04-04-2024, 04:25 PM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, 04-11-2024, 12:08 PM
    0 responses
    59 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    57 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    51 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-04-2024, 09:00 AM
    0 responses
    55 views
    0 likes
    Last Post seqadmin  
    Working...
    X