The SNP Translation dialog, accessible from the Variants track, displays the effect of variants (SNPs or indels) on annotation transcripts; it also allows for selection of heterozygous alleles and their effect on protein translation.

 1  Transcripts panel: Shows all transcripts whose CDS regions intersect the interval that was selected on the Variants track; this includes transcripts belonging to hidden Annotation tracks. The name of each transcript is displayed on the left-hand side; move the mouse over this label to see a tooltip with the transcript's full name and other statistics:

Transcript names are abbreviated by default, although you can change this behavior in the Options panel, as described below. 

If some of the transcripts do not fit in the panel, you can use the scroll bar on the right-hand side to scroll through them; alternatively, you can position the mouse over the panel and roll the Mouse wheel, or click and drag the panel with the Left mouse button.

The currently selected transcript is marked with a triangle icon (Triangle). You can click another transcript to select it instead; as you do, panel may zoom in or out slightly to accommodate it, and it will also automatically scroll (if needed) to position the newly selected transcript at the top:

The sequence of the currently selected transcript will be used as the source for protein translation, as described below.

 2  Samples panel: Shows all samples that are currently selected in the Variants dialog. The sample names are shown on the left-hand side, just like transcript names; similarly, you can scroll through the samples by using the scroll bar, rolling the Mouse wheel, or dragging inside the panel. You can also move the mouse over the sample name labels to expand them (assuming the names are abbreviated).

The variants for each sample are drawn using the same colors as on the Variants track: blue for homozygous variants that are identical to reference, red for homozygous variants that are different from the reference, and green for heterozygous variants. In addition, variants that change the protein translation are marked with a "flag" icon. A solid red flag denotes variant that changes the translation; a hollow white flag denotes a heterozygous variant only some of whose alleles affect the translation. You can see some examples of these variants in the screenshots above:
        Homozygous, same as reference
        Homozygous, different from reference, synonymous
        Heterozygous, all alleles are synonymous
        Homozygous, non-synonynous
        Heterozygous, some alleles are non-synonymous (but synonymous alleles are also present).

Exon boundaries are indicated with a  light gray  background; variants that occur outside of exons are hidden.

Click a variant to select it. The Translation panel will scroll to the selected variant, and the variant will be highlighted in yellow:

 3  Alignment panel: Connects variants on the Samples panel to their corresponding codons in the Translation panel below with dark blue lines. Exon boundaries of the currently selected transcript are outlined in teal. You can drag inside this panel (with the Left mouse button) to pan the view.

 4  Translation panel: Shows the current protein translation. The top line displays the reference sequence; the bottom line displays the DNA sequence resulting from the effects of the currently selected sample, alongside its corresponding protein. DNA codons are shown using alternating blue/black colors; nucleotides affected by variants that are different from reference are drawn on a  red  background; and if they happen to change protein translation, the corresponding aminoacid is likewise rendered on top of a  red  background. Variants that are identical to reference are outlined with a gray border:

The bar at the top of this panel outlines exon boundaries for the currently selected transcript in alternating  yellow  /  green  colors:

You can mouse over a variant to display a tooltip with its contents; the corresponding nucleotide will also be outlined in  sea green : 

Click the variant to show its allele switcher, where you can choose which of its alleles should be used for protein translation (naturally, this choice is only meaningful for heterozygous variants). In this example, the first allele (g) is identical to the reference; but the second allele (t) is different from reference, and also changes the translation. The number (in parentheses) after each allele indicates its dosage (which could only be 1 or 2 for diploid variants). By default, the allele with the highest dosage will be selected, but you can click the radio button next to another allele to use it instead:

       

As soon as you select the allele, the protein translation will change, and the corresponding "flag" will turn solid red (). The changed nucleotide will also be underlined, indicating that the allele affecting its translation was manually switched. You can keep switching alleles to mix-and-match them; for example:

Note that some variants might introduce a premature stop codon into the translation. In this case, any downstream variants will have no effect (since they will never be translated):

       

 5  Options: Here, you can customize miscellaneous display options for this dialog.

  • Name: Choose Smart (the default) to automatically abbreviate long transcript/sample names; Choose Full to always display the full names; or choose None to hide the names completely.
  • Hide switcher for homozygous SNPs: Only display the allele switcher for heterozygous variants; clicking a homozygous variant will have no effect.
  • Hide SNPs identical to Ref: In the Translation panel, completely hide variants that are identical to the reference (instead of outlining them with a gray border, as described above). 
  • Restore original alleles: Click and hold this button and it will begin filling in with a solid color from left to right. When the button fills in completely, all of your allele switcher selections will be cleared, resetting all heterozygous variants to their default alleles (i.e. the highest-dosage alleles for polyploid variants).