Unique variants in gene KLF14

Information The variants shown are described using the NM_138693.2 transcript reference sequence.

25 entries on 1 page. Showing entries 1 - 25.
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Reported     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
1 c.306G>C r.(?) p.(Glu102Asp) g.130418555C>G Copied from the Exome Variant Server KLF14_000025 1/12386 0/8256 1/4130
1 c.336C>T r.(=) p.(=) g.130418525G>A Copied from the Exome Variant Server KLF14_000024 4585/12590 3856/8364 729/4226
1 c.355C>T r.(?) p.(Pro119Ser) g.130418506G>A Copied from the Exome Variant Server KLF14_000023 658/12590 28/8380 630/4210
1 c.459G>T r.(=) p.(=) g.130418402C>A Copied from the Exome Variant Server KLF14_000022 108/10088 94/6826 14/3262
1 c.474_475insT r.(?) p.(Ala159Cysfs*64) g.130418386_130418387insA Copied from the Exome Variant Server KLF14_000021 15/9500 12/6438 3/3062
1 c.482del r.(?) p.(Ala161Glufs*11) g.130418379del Copied from the Exome Variant Server KLF14_000020 13/10040 11/6768 2/3272
1 c.517G>C r.(?) p.(Ala173Pro) g.130418344C>G Copied from the Exome Variant Server KLF14_000019 545/11830 21/7882 524/3948
1 c.551G>A r.(?) p.(Arg184Gln) g.130418310C>T Copied from the Exome Variant Server KLF14_000018 1/12834 1/8492 0/4342
1 c.568C>T r.(?) p.(Pro190Ser) g.130418293G>A Copied from the Exome Variant Server KLF14_000017 1/12986 0/8588 1/4398
1 c.603C>T r.(=) p.(=) g.130418258G>A Copied from the Exome Variant Server KLF14_000016 1/13002 1/8598 0/4404
1 c.638A>G r.(?) p.(Lys213Arg) g.130418223T>C Copied from the Exome Variant Server KLF14_000015 1/13006 1/8600 0/4406
1 c.659C>G r.(?) p.(Thr220Arg) g.130418202G>C Copied from the Exome Variant Server KLF14_000014 1/13006 1/8600 0/4406
1 c.671C>A r.(?) p.(Pro224His) g.130418190G>T Copied from the Exome Variant Server KLF14_000013 1/13006 1/8600 0/4406
1 c.681C>T r.(=) p.(=) g.130418180G>A Copied from the Exome Variant Server KLF14_000012 1/13006 1/8600 0/4406
1 c.813C>T r.(=) p.(=) g.130418048G>A Copied from the Exome Variant Server KLF14_000011 1/13004 1/8598 0/4406
1 c.827G>A r.(?) p.(Arg276His) g.130418034C>T Copied from the Exome Variant Server KLF14_000010 1/13004 1/8598 0/4406
1 c.832C>T r.(?) p.(Pro278Ser) g.130418029G>A Copied from the Exome Variant Server KLF14_000009 1/13004 1/8598 0/4406
1 c.864G>A r.(=) p.(=) g.130417997C>T Copied from the Exome Variant Server KLF14_000008 1/12974 0/8582 1/4392
1 c.867A>T r.(=) p.(=) g.130417994T>A Copied from the Exome Variant Server KLF14_000007 2/12976 0/8586 2/4390
1 c.933C>G r.(=) p.(=) g.130417928G>C Copied from the Exome Variant Server KLF14_000006 386/13004 7/8598 379/4406
1 c.940G>T r.(?) p.(Gly314Cys) g.130417921C>A Copied from the Exome Variant Server KLF14_000005 1/13006 1/8600 0/4406
1 c.948_949insGCG r.(?) p.(Ala316dup) g.130417912_130417913insCGC Copied from the Exome Variant Server KLF14_000004 8/12518 0/8254 8/4264
1 c.*18G>A r.(=) p.(=) g.130417871C>T Copied from the Exome Variant Server KLF14_000003 1/13004 0/8598 1/4406
1 c.*29A>G r.(=) p.(=) g.130417860T>C Copied from the Exome Variant Server KLF14_000002 2/13002 1/8596 1/4406
1 c.*48G>T r.(=) p.(=) g.130417841C>A Copied from the Exome Variant Server KLF14_000001 2/13004 2/8598 0/4406
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