Unique variants in gene PRRG3

Information The variants shown are described using the NM_024082.3 transcript reference sequence.

49 entries on 1 page. Showing entries 1 - 49.
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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.7+28C>T r.(=) p.(=) g.150867321C>T Copied from the Exome Variant Server PRRG3_000001 2876/10563 2672/6728 204/3835
1 c.7+46G>C r.(=) p.(=) g.150867339G>C Copied from the Exome Variant Server PRRG3_000002 3/10563 3/6728 0/3835
1 c.7+51T>G r.(=) p.(=) g.150867344T>G Copied from the Exome Variant Server PRRG3_000003 1/10563 1/6728 0/3835
1 c.7+94A>T r.(=) p.(=) g.150867387A>T Copied from the Exome Variant Server PRRG3_000004 247/3600 195/2391 52/1209
1 c.7+95del r.(=) p.(=) g.150867388del Copied from the Exome Variant Server PRRG3_000005 21/10191 18/6476 3/3715
1 c.8-44T>A r.(=) p.(=) g.150868424T>A Copied from the Exome Variant Server PRRG3_000006 2/10563 2/6728 0/3835
1 c.99G>T r.(?) p.(Glu33Asp) g.150868559G>T Copied from the Exome Variant Server PRRG3_000007 1/10563 1/6728 0/3835
1 c.101G>A r.(?) p.(Arg34Gln) g.150868561G>A Copied from the Exome Variant Server PRRG3_000008 1/10563 1/6728 0/3835
1 c.129C>T r.(=) p.(=) g.150868589C>T Copied from the Exome Variant Server PRRG3_000009 1/10563 0/6728 1/3835
1 c.168+12C>T r.(=) p.(=) g.150868640C>T Copied from the Exome Variant Server PRRG3_000010 7/10563 0/6728 7/3835
1 c.168+18G>A r.(=) p.(=) g.150868646G>A Copied from the Exome Variant Server PRRG3_000011 1/10563 0/6728 1/3835
1 c.168+22G>T r.(=) p.(=) g.150868650G>T Copied from the Exome Variant Server PRRG3_000012 8/10563 4/6728 4/3835
1 c.168+27G>C r.(=) p.(=) g.150868655G>C Copied from the Exome Variant Server PRRG3_000013 1/10563 1/6728 0/3835
1 c.214G>T r.(?) p.(Asp72Tyr) g.150869023G>T Copied from the Exome Variant Server PRRG3_000014 2/10563 2/6728 0/3835
1 c.223C>G r.(?) p.(Gln75Glu) g.150869032C>G Copied from the Exome Variant Server PRRG3_000015 1/10563 0/6728 1/3835
1 c.301T>C r.(?) p.(Trp101Arg) g.150869110T>C Copied from the Exome Variant Server PRRG3_000016 2/10563 2/6728 0/3835
1 c.318G>A r.(=) p.(=) g.150869127G>A Copied from the Exome Variant Server PRRG3_000017 125/10563 91/6728 34/3835
1 c.323C>T r.(?) p.(Ala108Val) g.150869132C>T Copied from the Exome Variant Server PRRG3_000018 7/10563 2/6728 5/3835
1 c.355C>T r.(?) p.(Arg119Trp) g.150869164C>T Copied from the Exome Variant Server PRRG3_000019 1/10563 1/6728 0/3835
1 c.370C>T r.(?) p.(Arg124Cys) g.150869179C>T Copied from the Exome Variant Server PRRG3_000020 3/10563 0/6728 3/3835
1 c.375C>T r.(=) p.(=) g.150869184C>T Copied from the Exome Variant Server PRRG3_000021 1/10563 0/6728 1/3835
1 c.382A>G r.(?) p.(Thr128Ala) g.150869191A>G Copied from the Exome Variant Server PRRG3_000022 3/10563 0/6728 3/3835
1 c.392G>A r.(?) p.(Arg131Gln) g.150869201G>A Copied from the Exome Variant Server PRRG3_000023 1/10563 0/6728 1/3835
1 c.421A>T r.(?) p.(Ser141Cys) g.150869230A>T Copied from the Exome Variant Server PRRG3_000024 1/10563 0/6728 1/3835
1 c.449A>G r.(?) p.(Glu150Gly) g.150869258A>G Copied from the Exome Variant Server PRRG3_000025 1/10563 1/6728 0/3835
1 c.458A>G r.(?) p.(Asn153Ser) g.150869267A>G Copied from the Exome Variant Server PRRG3_000028 9471/10563 6284/6728 3187/3835
1 c.464C>T r.(?) p.(Pro155Leu) g.150869273C>T Copied from the Exome Variant Server PRRG3_000029 48/10561 43/6726 5/3835
1 c.471G>A r.(=) p.(=) g.150869280G>A Copied from the Exome Variant Server PRRG3_000030 3/10559 0/6724 3/3835
1 c.488G>A r.(?) p.(Arg163Gln) g.150869297G>A Copied from the Exome Variant Server PRRG3_000031 64/10559 0/6725 64/3834
1 c.504A>G r.(=) p.(=) g.150869313A>G Copied from the Exome Variant Server PRRG3_000032 2/10561 2/6727 0/3834
1 c.508C>T r.(?) p.(Arg170Trp) g.150869317C>T Copied from the Exome Variant Server PRRG3_000033 3/10561 2/6727 1/3834
1 c.509G>T r.(?) p.(Arg170Leu) g.150869318G>T Copied from the Exome Variant Server PRRG3_000034 2/10561 0/6727 2/3834
1 c.516G>C r.(?) p.(Glu172Asp) g.150869325G>C Copied from the Exome Variant Server PRRG3_000035 1/10561 0/6727 1/3834
1 c.522C>A r.(=) p.(=) g.150869331C>A Copied from the Exome Variant Server PRRG3_000036 1/10562 0/6728 1/3834
1 c.538C>T r.(?) p.(Leu180Phe) g.150869347C>T Copied from the Exome Variant Server PRRG3_000037 92/10562 0/6728 92/3834
1 c.542C>G r.(?) p.(Ser181Cys) g.150869351C>G Copied from the Exome Variant Server PRRG3_000038 1/10562 1/6728 0/3834
1 c.554T>G r.(?) p.(Leu185Arg) g.150869363T>G Copied from the Exome Variant Server PRRG3_000039 1/10563 1/6728 0/3835
1 c.596C>T r.(?) p.(Ala199Val) g.150869405C>T Copied from the Exome Variant Server PRRG3_000040 1/10563 0/6728 1/3835
1 c.606G>A r.(=) p.(=) g.150869415G>A Copied from the Exome Variant Server PRRG3_000041 3/10563 3/6728 0/3835
1 c.627C>T r.(=) p.(=) g.150869436C>T Copied from the Exome Variant Server PRRG3_000042 17/10563 1/6728 16/3835
1 c.628G>A r.(?) p.(Val210Met) g.150869437G>A Copied from the Exome Variant Server PRRG3_000043 2/10563 2/6728 0/3835
1 c.646C>T r.(?) p.(Pro216Ser) g.150869455C>T Copied from the Exome Variant Server PRRG3_000044 1/10563 1/6728 0/3835
1 c.672C>T r.(=) p.(=) g.150869481C>T Copied from the Exome Variant Server PRRG3_000045 2/10563 2/6728 0/3835
1 c.673G>T r.(?) p.(Ala225Ser) g.150869482G>T Copied from the Exome Variant Server PRRG3_000046 1/10563 0/6728 1/3835
1 c.675C>T r.(=) p.(=) g.150869484C>T Copied from the Exome Variant Server PRRG3_000047 24/10563 0/6728 24/3835
1 c.685G>A r.(?) p.(Ala229Thr) g.150869494G>A Copied from the Exome Variant Server PRRG3_000048 26/10561 0/6726 26/3835
1 c.*26T>A r.(=) p.(=) g.150869531T>A Copied from the Exome Variant Server PRRG3_000049 1/10562 1/6727 0/3835
1 c.*40C>T r.(=) p.(=) g.150869545C>T Copied from the Exome Variant Server PRRG3_000027 2/10562 1/6727 1/3835
1 c.*44G>T r.(=) p.(=) g.150869549G>T Copied from the Exome Variant Server PRRG3_000026 1/10557 1/6725 0/3832
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