GET-Evidence: Search

 
VariantImpactInheritance patternSummaryGenomes
FANCG E105Xinsufficiently evaluated pathogenicunknown

(19 web hits)

FANCG R214Cinsufficiently evaluated not reviewed, f=0.004unknown var-GS19026-1100-36-ASM
FANCG T297Iinsufficiently evaluated not reviewed, f=0.030unknown var-GS19701-1100-36-ASM
var-GS19239-1100-36-ASM
var-GS18502-1100-36-ASM
var-GS18505-1100-36-ASM
FANCG Q356Xinsufficiently evaluated pathogenicunknown

(8 web hits)

FANCG S378Linsufficiently evaluated none, f=0.036unknown

(10 web hits)

var-GS19020-1100-36-ASM
var-GS19129-1100-36-ASM
var-GS18505-1100-36-ASM
var-GS18517-1100-36-ASM
FANCG R485Qinsufficiently evaluated not reviewed, f=0.008unknown var-GS18502-1100-36-ASM
FANCG R513Quncertain pathogenic, f=0.007dominant

Rare polymorphism. Hypothesized to increase susceptibility to childhood acute myeloid leukemia, but the numbers in the study failed to have statistical significance.

(14 web hits)

CGI sample GS00253-DNA_E01_200_37
Total results: 7

Gene search

"GENE" or "GENE A123C":

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