All transcript variants in gene RHOXF2

Information The variants shown are described using the NM_032498.1 transcript reference sequence.

24 entries on 1 page. Showing entries 1 - 24.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.186G>A r.(=) p.(=) g.119293027G>A Copied from the Exome Variant Server RHOXF2_000001 6/7468 6/4933 0/2535
?/? c.199_219del r.(?) p.(Glu76_Gly82del) g.119293040_119293060del Copied from the Exome Variant Server RHOXF2_000002 134/5306 78/3428 56/1878
?/? c.202G>A r.(?) p.(Gly68Arg) g.119293043G>A Copied from the Exome Variant Server RHOXF2_000003 38/8291 34/5422 4/2869
?/? c.219C>T r.(=) p.(=) g.119293060C>T Copied from the Exome Variant Server RHOXF2_000005 2/8672 0/5614 2/3058
?/? c.243C>T r.(=) p.(=) g.119293084C>T Copied from the Exome Variant Server RHOXF2_000007 18/10497 0/6714 18/3783
?/? c.244G>A r.(?) p.(Gly82Ser) g.119293085G>A Copied from the Exome Variant Server RHOXF2_000009 4/10496 1/6713 3/3783
?/? c.247G>A r.(?) p.(Ala83Thr) g.119293088G>A Copied from the Exome Variant Server RHOXF2_000011 61/10498 1/6715 60/3783
?/? c.256C>T r.(?) p.(Pro86Ser) g.119293097C>T Copied from the Exome Variant Server RHOXF2_000013 1/10496 0/6715 1/3781
?/? c.267A>G r.(=) p.(=) g.119293108A>G Copied from the Exome Variant Server RHOXF2_000015 169/10497 2/6715 167/3782
?/? c.282C>T r.(=) p.(=) g.119293123C>T Copied from the Exome Variant Server RHOXF2_000017 12/10495 12/6714 0/3781
?/? c.283G>A r.(?) p.(Glu95Lys) g.119293124G>A Copied from the Exome Variant Server RHOXF2_000019 1/10497 0/6714 1/3783
?/? c.295G>A r.(?) p.(Gly99Ser) g.119293136G>A Copied from the Exome Variant Server RHOXF2_000004 1/10503 0/6714 1/3789
?/? c.301G>A r.(?) p.(Asp101Asn) g.119293142G>A Copied from the Exome Variant Server RHOXF2_000006 1/10505 1/6713 0/3792
?/? c.315G>A r.(=) p.(=) g.119293156G>A Copied from the Exome Variant Server RHOXF2_000008 28/10510 1/6716 27/3794
?/? c.321C>T r.(=) p.(=) g.119293162C>T Copied from the Exome Variant Server RHOXF2_000010 2/10503 2/6710 0/3793
?/? c.375_376insG r.(?) p.(Leu128Alafs*34) g.119293216_119293217insG Copied from the Exome Variant Server RHOXF2_000012 88/9397 77/5936 11/3461
?/? c.399G>A r.(=) p.(=) g.119293240G>A Copied from the Exome Variant Server RHOXF2_000014 3/10419 3/6634 0/3785
?/? c.411C>T r.(=) p.(=) g.119293252C>T Copied from the Exome Variant Server RHOXF2_000016 13/10531 10/6705 3/3826
?/? c.417C>T r.(=) p.(=) g.119293258C>T Copied from the Exome Variant Server RHOXF2_000018 1/10546 0/6719 1/3827
?/? c.429A>G r.(=) p.(=) g.119293270A>G Copied from the Exome Variant Server RHOXF2_000020 5/10550 0/6722 5/3828
?/? c.452G>A r.(?) p.(Arg151His) g.119293293G>A Copied from the Exome Variant Server RHOXF2_000021 152/10550 2/6722 150/3828
?/? c.463C>T r.(?) p.(Arg155Cys) g.119293304C>T Copied from the Exome Variant Server RHOXF2_000022 1/10550 0/6722 1/3828
?/? c.491+10T>C r.(=) p.(=) g.119293342T>C Copied from the Exome Variant Server RHOXF2_000023 191/10419 1/6641 190/3778
?/? c.491+27C>T r.(=) p.(=) g.119293359C>T Copied from the Exome Variant Server RHOXF2_000024 1/10454 1/6644 0/3810
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