Note: This variant has not been sufficiently evaluated by a GET-Evidence editor.
To be considered sufficiently evaluated a variant must have both "variant evidence" and "clinical importance" scores filled in.
Please help improve GET-Evidence by evaluating evidence for this variant!
(SLFN13 Lys658Asn)
You are viewing an old version of this page that was saved on March 29, 2011 at 8:55pm by Genome Importing Robot.
Short summary
Impact
Insufficiently evaluated not reviewed
(The "insufficiently evaluated" qualifier is assigned automatically based on the above evidence and importance scores.)
Inheritance pattern
unknown
Summary of published research, and additional commentary
hu0D879F - CGI sample GS00253-DNA_G01_200_37 het G @ chr17:33768334
hu43860C - CGI sample GS00253-DNA_A01_200_37 het G @ chr17:33768334
hu604D39 - CGI sample GS00253-DNA_B02_200_37 het G @ chr17:33768334
huAE6220 - CGI sample GS00253-DNA_H01_200_37 het G @ chr17:33768334
Added in this revision:
GS18504 - var-GS18504-1100-36-ASM hom G @ chr17:30792447
GS18505 - var-GS18505-1100-36-ASM het G @ chr17:30792447
NA19240
snp-1