FANCG gene mutations are not reported systematically from Indian FA patients. C.1143 + 5 G > C mutation of intron9 causes exon9 skipping and can hamper TPR3 motif. C.883dupG mutation causes truncation before TPR3 motif and remainder C-terminus. Del-ins mutation c.1471_1473delAAAinsG hampers TPR6 and the remainder C-terminus.