Unique variants in gene PRCD

Information The variants shown are described using the NM_001077620.2 transcript reference sequence.

32 entries on 1 page. Showing entries 1 - 32.
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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.-2786C>G r.(=) p.(=) g.74533438C>G Copied from the Exome Variant Server CYGB_000044 92/12676 0/8372 92/4304
1 c.-2713G>A r.(=) p.(=) g.74533511G>A Copied from the Exome Variant Server CYGB_000046 3/13006 0/8600 3/4406
1 c.-2703T>C r.(?) p.(Tyr35Cys) g.74533521T>C Copied from the Exome Variant Server CYGB_000048 1/13006 1/8600 0/4406
1 c.-2701G>C r.(=) p.(=) g.74533523G>C Copied from the Exome Variant Server CYGB_000050 2/13006 2/8600 0/4406
1 c.-2677C>T r.(=) p.(=) g.74533547C>T Copied from the Exome Variant Server CYGB_000051 1/13006 0/8600 1/4406
1 c.-2642G>C r.(?) p.(Arg15Gly) g.74533582G>C Copied from the Exome Variant Server CYGB_000052 1/13006 0/8600 1/4406
1 c.-2626C>A r.(?) p.(Glu9Asp) g.74533598C>A Copied from the Exome Variant Server CYGB_000053 1/13006 0/8600 1/4406
1 c.-38T>C r.(=) p.(=) g.74536186T>C Copied from the Exome Variant Server PRCD_000001 1/12220 0/8288 1/3932
1 c.13C>G r.(?) p.(Leu5Val) g.74536236C>G Copied from the Exome Variant Server PRCD_000002 3/12398 3/8346 0/4052
1 c.49C>T r.(?) p.(Arg17Cys) g.74536272C>T Copied from the Exome Variant Server PRCD_000003 1/12220 1/8302 0/3918
1 c.74+14C>T r.(=) p.(=) g.74536311C>T Copied from the Exome Variant Server PRCD_000004 42/11924 1/8186 41/3738
1 c.74+21T>C r.(=) p.(=) g.74536318T>C Copied from the Exome Variant Server PRCD_000005 44/11808 0/8142 44/3666
1 c.74+35del r.(=) p.(=) g.74536332del Copied from the Exome Variant Server PRCD_000006 838/10170 581/7090 257/3080
1 c.74+35_74+36del r.(=) p.(=) g.74536332_74536333del Copied from the Exome Variant Server PRCD_000007 3516/10170 2449/7090 1067/3080
1 c.74+37_74+38del r.(=) p.(=) g.74536334_74536335del Copied from the Exome Variant Server PRCD_000008 307/6072 146/4406 161/1666
1 c.74+37_74+38insT r.(=) p.(=) g.74536334_74536335insT Copied from the Exome Variant Server PRCD_000009 140/9772 85/6818 55/2954
1 c.74+38del r.(=) p.(=) g.74536335del Copied from the Exome Variant Server PRCD_000010 300/6072 141/4406 159/1666
1 c.74+39_74+40insC r.(=) p.(=) g.74536336_74536337insC Copied from the Exome Variant Server PRCD_000011 1046/9132 949/6370 97/2762
1 c.74+40G>C r.(=) p.(=) g.74536337G>C Copied from the Exome Variant Server PRCD_000012 178/9590 165/6686 13/2904
1 c.74+42_74+43insC r.(=) p.(=) g.74536339_74536340insC Copied from the Exome Variant Server PRCD_000013 65/8354 52/5816 13/2538
1 c.74+49dup r.(=) p.(=) g.74536346dup Copied from the Exome Variant Server PRCD_000014 170/7468 46/5216 124/2252
1 c.74+49_74+51del r.(=) p.(=) g.74536346_74536348del Copied from the Exome Variant Server PRCD_000015 274/7468 213/5216 61/2252
1 c.75-63T>C r.(=) p.(=) g.74536524T>C Copied from the Exome Variant Server PRCD_000016 2/4566 1/3182 1/1384
1 c.85G>A r.(?) p.(Asp29Asn) g.74536597G>A Copied from the Exome Variant Server PRCD_000017 3/12388 1/8354 2/4034
1 c.95G>T r.(?) p.(Gly32Val) g.74536607G>T Copied from the Exome Variant Server PRCD_000018 3/12506 0/8390 3/4116
1 c.109A>G r.(?) p.(Ser37Gly) g.74536621A>G Copied from the Exome Variant Server PRCD_000019 1/12616 0/8412 1/4204
1 c.144-50T>G r.(=) p.(=) g.74538585T>G Copied from the Exome Variant Server PRCD_000020 16/12372 14/8338 2/4034
1 c.144-41C>T r.(=) p.(=) g.74538594C>T Copied from the Exome Variant Server PRCD_000021 2/12352 2/8336 0/4016
1 c.144-40G>A r.(=) p.(=) g.74538595G>A Copied from the Exome Variant Server PRCD_000022 1/12346 1/8336 0/4010
1 c.144-20C>T r.(=) p.(=) g.74538615C>T Copied from the Exome Variant Server PRCD_000023 1/12272 1/8320 0/3952
1 c.164A>C r.(?) p.(*55Serext*49) g.74538655A>C Copied from the Exome Variant Server PRCD_000024 1/12198 1/8286 0/3912
1 c.*59+21G>A r.(=) p.(=) g.74538736G>A Copied from the Exome Variant Server PRCD_000025 1/4566 1/3182 0/1384
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