All transcript variants in gene FAM155B

Information The variants shown are described using the NM_015686.2 transcript reference sequence.

47 entries on 1 page. Showing entries 1 - 47.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.54_56del r.(?) p.(Cys24del) g.68725179_68725181del Copied from the Exome Variant Server FAM155B_000001 682/7990 381/4986 301/3004
?/? c.104C>T r.(?) p.(Ala35Val) g.68725229C>T Copied from the Exome Variant Server FAM155B_000002 1/9153 1/5771 0/3382
?/? c.297_299del r.(?) p.(Pro104del) g.68725422_68725424del Copied from the Exome Variant Server FAM155B_000003 16/1379 8/979 8/400
?/? c.347C>T r.(?) p.(Pro116Leu) g.68725472C>T Copied from the Exome Variant Server FAM155B_000004 3/8480 3/5676 0/2804
?/? c.471C>T r.(=) p.(=) g.68725596C>T Copied from the Exome Variant Server FAM155B_000005 3/10524 3/6711 0/3813
?/? c.476C>T r.(?) p.(Pro159Leu) g.68725601C>T Copied from the Exome Variant Server FAM155B_000006 12/10520 4/6711 8/3809
?/? c.515T>C r.(?) p.(Leu172Pro) g.68725640T>C Copied from the Exome Variant Server FAM155B_000007 5415/10556 2199/6725 3216/3831
?/? c.531C>A r.(=) p.(=) g.68725656C>A Copied from the Exome Variant Server FAM155B_000008 1/10563 1/6728 0/3835
?/? c.612C>T r.(=) p.(=) g.68725737C>T Copied from the Exome Variant Server FAM155B_000009 1/10562 1/6728 0/3834
?/? c.622C>T r.(=) p.(=) g.68725747C>T Copied from the Exome Variant Server FAM155B_000010 1/10563 1/6728 0/3835
?/? c.660C>T r.(=) p.(=) g.68725785C>T Copied from the Exome Variant Server FAM155B_000011 1/10563 1/6728 0/3835
?/? c.670C>G r.(?) p.(Leu224Val) g.68725795C>G Copied from the Exome Variant Server FAM155B_000012 47/10563 0/6728 47/3835
?/? c.676G>T r.(?) p.(Gly226Trp) g.68725801G>T Copied from the Exome Variant Server FAM155B_000013 2/10563 2/6728 0/3835
?/? c.681C>G r.(?) p.(Asp227Glu) g.68725806C>G Copied from the Exome Variant Server FAM155B_000014 1/10563 0/6728 1/3835
?/? c.691G>A r.(?) p.(Val231Met) g.68725816G>A Copied from the Exome Variant Server FAM155B_000015 8/10554 0/6723 8/3831
?/? c.699C>T r.(=) p.(=) g.68725824C>T Copied from the Exome Variant Server FAM155B_000016 1/10557 1/6724 0/3833
?/? c.746C>T r.(?) p.(Ala249Val) g.68725871C>T Copied from the Exome Variant Server FAM155B_000017 1/10561 1/6728 0/3833
?/? c.798C>T r.(=) p.(=) g.68725923C>T Copied from the Exome Variant Server FAM155B_000018 1/10563 0/6728 1/3835
?/? c.805C>T r.(?) p.(His269Tyr) g.68725930C>T Copied from the Exome Variant Server FAM155B_000019 1/10563 1/6728 0/3835
?/? c.813C>T r.(=) p.(=) g.68725938C>T Copied from the Exome Variant Server FAM155B_000020 1/10563 0/6728 1/3835
?/? c.861+6G>A r.(=) p.(=) g.68725992G>A Copied from the Exome Variant Server FAM155B_000021 2/10549 2/6722 0/3827
?/? c.861+9T>A r.(=) p.(=) g.68725995T>A Copied from the Exome Variant Server FAM155B_000022 1/10543 1/6716 0/3827
?/? c.908A>C r.(?) p.(Gln303Pro) g.68748882A>C Copied from the Exome Variant Server FAM155B_000023 1/10563 0/6728 1/3835
?/? c.942A>T r.(?) p.(Gln314His) g.68748916A>T Copied from the Exome Variant Server FAM155B_000024 1/10563 0/6728 1/3835
?/? c.965G>A r.(?) p.(Arg322Gln) g.68748939G>A Copied from the Exome Variant Server FAM155B_000025 1/10563 1/6728 0/3835
?/? c.984C>T r.(=) p.(=) g.68748958C>T Copied from the Exome Variant Server FAM155B_000026 2/10563 1/6728 1/3835
?/? c.1033+11G>T r.(=) p.(=) g.68749018G>T Copied from the Exome Variant Server FAM155B_000027 1/10563 1/6728 0/3835
?/? c.1033+35C>T r.(=) p.(=) g.68749042C>T Copied from the Exome Variant Server FAM155B_000028 1/10558 1/6723 0/3835
?/? c.1033+36G>A r.(=) p.(=) g.68749043G>A Copied from the Exome Variant Server FAM155B_000029 1/10556 0/6723 1/3833
?/? c.1034-35G>A r.(=) p.(=) g.68749379G>A Copied from the Exome Variant Server FAM155B_000030 4838/10562 3784/6727 1054/3835
?/? c.1034-8A>G r.(=) p.(=) g.68749406A>G Copied from the Exome Variant Server FAM155B_000031 1/10563 1/6728 0/3835
?/? c.1034-4G>T r.spl? p.? g.68749410G>T Copied from the Exome Variant Server FAM155B_000032 1/10563 1/6728 0/3835
?/? c.1103C>T r.(?) p.(Ala368Val) g.68749483C>T Copied from the Exome Variant Server FAM155B_000033 6/10563 0/6728 6/3835
?/? c.1104G>A r.(=) p.(=) g.68749484G>A Copied from the Exome Variant Server FAM155B_000034 1/10563 1/6728 0/3835
?/? c.1104_1109del r.(?) p.(Lys371_Lys372del) g.68749484_68749489del Copied from the Exome Variant Server FAM155B_000035 1/10205 0/6484 1/3721
?/? c.1116G>A r.(=) p.(=) g.68749496G>A Copied from the Exome Variant Server FAM155B_000036 1/10563 0/6728 1/3835
?/? c.1205_1206insC r.(?) p.(His404Profs*3) g.68749585_68749586insC Copied from the Exome Variant Server FAM155B_000037 2/10205 2/6484 0/3721
?/? c.1228C>T r.(?) p.(Arg410Cys) g.68749608C>T Copied from the Exome Variant Server FAM155B_000038 2/10563 2/6728 0/3835
?/? c.1229G>A r.(?) p.(Arg410His) g.68749609G>A Copied from the Exome Variant Server FAM155B_000039 2/10563 0/6728 2/3835
?/? c.1254G>A r.(=) p.(=) g.68749634G>A Copied from the Exome Variant Server FAM155B_000040 313/10563 0/6728 313/3835
?/? c.1256C>T r.(?) p.(Pro419Leu) g.68749636C>T Copied from the Exome Variant Server FAM155B_000041 1/10563 1/6728 0/3835
?/? c.1257G>A r.(=) p.(=) g.68749637G>A Copied from the Exome Variant Server FAM155B_000042 2/10563 1/6728 1/3835
?/? c.1294C>T r.(?) p.(Arg432Trp) g.68749674C>T Copied from the Exome Variant Server FAM155B_000043 1/10563 1/6728 0/3835
?/? c.1329C>T r.(=) p.(=) g.68749709C>T Copied from the Exome Variant Server FAM155B_000044 5/10563 5/6728 0/3835
?/? c.1379C>T r.(?) p.(Thr460Ile) g.68749759C>T Copied from the Exome Variant Server FAM155B_000045 11/10562 0/6727 11/3835
?/? c.1408C>T r.(?) p.(Arg470Trp) g.68749788C>T Copied from the Exome Variant Server FAM155B_000046 1/10561 0/6726 1/3835
?/? c.*37A>G r.(=) p.(=) g.68749836A>G Copied from the Exome Variant Server FAM155B_000047 5/10482 0/6661 5/3821
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