All transcript variants in gene TNFRSF17

Information The variants shown are described using the NM_001192.2 transcript reference sequence.

54 entries on 1 page. Showing entries 1 - 54.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.-5T>C r.(=) p.(=) g.12059177T>C Copied from the Exome Variant Server TNFRSF17_000001 1/12994 0/8600 1/4394
?/? c.33T>C r.(=) p.(=) g.12059214T>C Copied from the Exome Variant Server TNFRSF17_000002 6/12994 0/8600 6/4394
?/? c.55C>A r.(?) p.(His19Asn) g.12059236C>A Copied from the Exome Variant Server TNFRSF17_000003 1/12994 1/8600 0/4394
?/? c.57T>G r.(?) p.(His19Gln) g.12059238T>G Copied from the Exome Variant Server TNFRSF17_000004 1/12994 1/8600 0/4394
?/? c.58G>A r.(?) p.(Ala20Thr) g.12059239G>A Copied from the Exome Variant Server TNFRSF17_000005 1/12994 0/8600 1/4394
?/? c.80G>A r.(?) p.(Arg27Gln) g.12059261G>A Copied from the Exome Variant Server TNFRSF17_000006 4/12994 0/8600 4/4394
?/? c.97C>T r.(?) p.(Pro33Ser) g.12059278C>T Copied from the Exome Variant Server TNFRSF17_000007 2/12994 2/8600 0/4394
?/? c.102_104del r.(?) p.(Leu35del) g.12059283_12059285del Copied from the Exome Variant Server TNFRSF17_000008 2/12514 0/8250 2/4264
?/? c.130+16T>A r.(=) p.(=) g.12059327T>A Copied from the Exome Variant Server TNFRSF17_000009 1/12994 1/8600 0/4394
?/? c.130+17G>C r.(=) p.(=) g.12059328G>C Copied from the Exome Variant Server TNFRSF17_000010 2/12994 2/8600 0/4394
?/? c.130+21G>A r.(=) p.(=) g.12059332G>A Copied from the Exome Variant Server TNFRSF17_000011 1/12994 0/8600 1/4394
?/? c.130+48T>C r.(=) p.(=) g.12059359T>C Copied from the Exome Variant Server TNFRSF17_000012 1/12994 1/8600 0/4394
?/? c.131-44_131-40del r.(=) p.(=) g.12060008_12060012del Copied from the Exome Variant Server TNFRSF17_000013 2/12516 2/8254 0/4262
?/? c.131-29A>G r.(=) p.(=) g.12060023A>G Copied from the Exome Variant Server TNFRSF17_000014 138/12994 126/8600 12/4394
?/? c.131-25_131-22del r.(=) p.(=) g.12060027_12060030del Copied from the Exome Variant Server TNFRSF17_000015 13/12518 0/8254 13/4264
?/? c.131-22G>C r.(=) p.(=) g.12060030G>C Copied from the Exome Variant Server TNFRSF17_000017 1/12994 1/8600 0/4394
?/? c.131-17A>C r.(=) p.(=) g.12060035A>C Copied from the Exome Variant Server TNFRSF17_000019 2/12994 2/8600 0/4394
?/? c.131-16T>C r.(=) p.(=) g.12060036T>C Copied from the Exome Variant Server TNFRSF17_000021 1/12994 1/8600 0/4394
?/? c.131-8T>C r.(=) p.(=) g.12060044T>C Copied from the Exome Variant Server TNFRSF17_000016 1/12994 1/8600 0/4394
?/? c.151G>C r.(?) p.(Gly51Arg) g.12060072G>C Copied from the Exome Variant Server TNFRSF17_000018 1/12994 0/8600 1/4394
?/? c.155C>T r.(?) p.(Thr52Met) g.12060076C>T Copied from the Exome Variant Server TNFRSF17_000020 6/12994 0/8600 6/4394
?/? c.161C>T r.(?) p.(Ala54Val) g.12060082C>T Copied from the Exome Variant Server TNFRSF17_000022 3/12994 0/8600 3/4394
?/? c.176G>A r.(?) p.(Cys59Tyr) g.12060097G>A Copied from the Exome Variant Server TNFRSF17_000023 6/12994 6/8600 0/4394
?/? c.185T>G r.(?) p.(Leu62Arg) g.12060106T>G Copied from the Exome Variant Server TNFRSF17_000024 1/12994 1/8600 0/4394
?/? c.191_193del r.(?) p.(Ile66del) g.12060112_12060114del Copied from the Exome Variant Server TNFRSF17_000025 51/12518 31/8254 20/4264
?/? c.193A>G r.(?) p.(Ile65Val) g.12060114A>G Copied from the Exome Variant Server TNFRSF17_000026 19/12994 0/8600 19/4394
?/? c.194T>C r.(?) p.(Ile65Thr) g.12060115T>C Copied from the Exome Variant Server TNFRSF17_000027 1/12994 0/8600 1/4394
?/? c.214G>T r.(?) p.(Val72Leu) g.12060135G>T Copied from the Exome Variant Server TNFRSF17_000028 1/12994 0/8600 1/4394
?/? c.242A>G r.(?) p.(Asn81Ser) g.12060163A>G Copied from the Exome Variant Server TNFRSF17_000029 12450/12994 8499/8600 3951/4394
?/? c.260A>G r.(?) p.(Asp87Gly) g.12060181A>G Copied from the Exome Variant Server TNFRSF17_000030 1/12994 0/8600 1/4394
?/? c.276A>G r.(=) p.(=) g.12060197A>G Copied from the Exome Variant Server TNFRSF17_000031 1/12994 1/8600 0/4394
?/? c.277G>A r.(?) p.(Gly93Arg) g.12060198G>A Copied from the Exome Variant Server TNFRSF17_000032 1/12994 0/8600 1/4394
?/? c.277+5G>C r.spl? p.? g.12060203G>C Copied from the Exome Variant Server TNFRSF17_000033 1/12994 0/8600 1/4394
?/? c.277+21T>C r.(=) p.(=) g.12060219T>C Copied from the Exome Variant Server TNFRSF17_000034 1/12994 1/8600 0/4394
?/? c.277+38G>A r.(=) p.(=) g.12060236G>A Copied from the Exome Variant Server TNFRSF17_000035 29/12994 0/8600 29/4394
?/? c.278-20T>C r.(=) p.(=) g.12061407T>C Copied from the Exome Variant Server TNFRSF17_000036 1/12994 0/8600 1/4394
?/? c.278-17C>T r.(=) p.(=) g.12061410C>T Copied from the Exome Variant Server TNFRSF17_000037 2/12994 2/8600 0/4394
?/? c.278-6A>C r.(=) p.(=) g.12061421A>C Copied from the Exome Variant Server TNFRSF17_000038 1/12994 0/8600 1/4394
?/? c.301A>T r.(?) p.(Asn101Tyr) g.12061450A>T Copied from the Exome Variant Server TNFRSF17_000039 1/12994 1/8600 0/4394
?/? c.305T>C r.(?) p.(Ile102Thr) g.12061454T>C Copied from the Exome Variant Server TNFRSF17_000040 3/12994 0/8600 3/4394
?/? c.363C>G r.(?) p.(Tyr121*) g.12061512C>G Copied from the Exome Variant Server TNFRSF17_000041 1/12994 1/8600 0/4394
?/? c.365C>T r.(?) p.(Thr122Met) g.12061514C>T Copied from the Exome Variant Server TNFRSF17_000042 2/12994 2/8600 0/4394
?/? c.407C>T r.(?) p.(Pro136Leu) g.12061556C>T Copied from the Exome Variant Server TNFRSF17_000043 1/12994 0/8600 1/4394
?/? c.433C>T r.(?) p.(Pro145Ser) g.12061582C>T Copied from the Exome Variant Server TNFRSF17_000044 2/12994 2/8600 0/4394
?/? c.446T>G r.(?) p.(Met149Arg) g.12061595T>G Copied from the Exome Variant Server TNFRSF17_000045 8/12994 8/8600 0/4394
?/? c.456C>T r.(=) p.(=) g.12061605C>T Copied from the Exome Variant Server TNFRSF17_000046 36/12994 3/8600 33/4394
?/? c.457G>A r.(?) p.(Ala153Thr) g.12061606G>A Copied from the Exome Variant Server TNFRSF17_000047 3/12994 0/8600 3/4394
?/? c.477G>A r.(=) p.(=) g.12061626G>A Copied from the Exome Variant Server TNFRSF17_000048 1387/12994 447/8600 940/4394
?/? c.494G>C r.(?) p.(Cys165Ser) g.12061643G>C Copied from the Exome Variant Server TNFRSF17_000049 3/12994 1/8600 2/4394
?/? c.524C>T r.(?) p.(Thr175Met) g.12061673C>T Copied from the Exome Variant Server TNFRSF17_000050 2/12994 1/8600 1/4394
?/? c.525G>A r.(=) p.(=) g.12061674G>A Copied from the Exome Variant Server TNFRSF17_000051 566/12994 303/8600 263/4394
?/? c.528G>C r.(?) p.(Glu176Asp) g.12061677G>C Copied from the Exome Variant Server TNFRSF17_000052 70/12994 0/8600 70/4394
?/? c.*12G>A r.(=) p.(=) g.12061716G>A Copied from the Exome Variant Server TNFRSF17_000053 2/12994 0/8600 2/4394
?/? c.*22G>A r.(=) p.(=) g.12061726G>A Copied from the Exome Variant Server TNFRSF17_000054 1/12994 0/8600 1/4394
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