All transcript variants in gene FAM9B

Information The variants shown are described using the NM_205849.2 transcript reference sequence.

45 entries on 1 page. Showing entries 1 - 45.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.-70C>T r.(=) p.(=) g.9001097G>A Copied from the Exome Variant Server FAM9B_000045 1/3600 0/2391 1/1209
?/? c.27A>G r.(=) p.(=) g.9001001T>C Copied from the Exome Variant Server FAM9B_000044 1/10563 1/6728 0/3835
?/? c.28+27A>G r.(=) p.(=) g.9000973T>C Copied from the Exome Variant Server FAM9B_000043 1/10563 1/6728 0/3835
?/? c.28+49C>T r.(=) p.(=) g.9000951G>A Copied from the Exome Variant Server FAM9B_000042 2/10563 0/6728 2/3835
?/? c.28+50G>C r.(=) p.(=) g.9000950C>G Copied from the Exome Variant Server FAM9B_000041 10/10563 0/6728 10/3835
?/? c.28+59G>C r.(=) p.(=) g.9000941C>G Copied from the Exome Variant Server FAM9B_000040 3/3600 0/2391 3/1209
?/? c.29-41T>C r.(=) p.(=) g.9000543A>G Copied from the Exome Variant Server FAM9B_000039 36/10563 29/6728 7/3835
?/? c.29-12A>T r.(=) p.(=) g.9000514T>A Copied from the Exome Variant Server FAM9B_000038 1/10563 1/6728 0/3835
?/? c.41T>G r.(?) p.(Val14Gly) g.9000490A>C Copied from the Exome Variant Server FAM9B_000037 1/10563 0/6728 1/3835
?/? c.68G>A r.(?) p.(Arg23His) g.9000463C>T Copied from the Exome Variant Server FAM9B_000036 2/10563 2/6728 0/3835
?/? c.149+33T>C r.(=) p.(=) g.9000349A>G Copied from the Exome Variant Server FAM9B_000035 1/10563 0/6728 1/3835
?/? c.181+1G>A r.spl? p.? g.9000170C>T Copied from the Exome Variant Server FAM9B_000034 1/10560 1/6727 0/3833
?/? c.181+11G>A r.(=) p.(=) g.9000160C>T Copied from the Exome Variant Server FAM9B_000033 1/10557 0/6724 1/3833
?/? c.181+47A>G r.(=) p.(=) g.9000124T>C Copied from the Exome Variant Server FAM9B_000032 1/10555 1/6721 0/3834
?/? c.182-48A>G r.(=) p.(=) g.8998449T>C Copied from the Exome Variant Server FAM9B_000031 50/10478 0/6681 50/3797
?/? c.182-21A>G r.(=) p.(=) g.8998422T>C Copied from the Exome Variant Server FAM9B_000030 2/10531 2/6713 0/3818
?/? c.191C>T r.(?) p.(Thr64Ile) g.8998392G>A Copied from the Exome Variant Server FAM9B_000029 2/10548 0/6722 2/3826
?/? c.276T>G r.(=) p.(=) g.8998307A>C Copied from the Exome Variant Server FAM9B_000028 1/10540 0/6715 1/3825
?/? c.281+29A>G r.(=) p.(=) g.8998273T>C Copied from the Exome Variant Server FAM9B_000027 1/10513 0/6697 1/3816
?/? c.281+47T>C r.(=) p.(=) g.8998255A>G Copied from the Exome Variant Server FAM9B_000026 1/10468 1/6667 0/3801
?/? c.282-31G>A r.(=) p.(=) g.8997490C>T Copied from the Exome Variant Server FAM9B_000025 1/10559 0/6726 1/3833
?/? c.282-24C>T r.(=) p.(=) g.8997483G>A Copied from the Exome Variant Server FAM9B_000024 19/10561 18/6726 1/3835
?/? c.282-23G>A r.(=) p.(=) g.8997482C>T Copied from the Exome Variant Server FAM9B_000023 4/10561 4/6726 0/3835
?/? c.301C>T r.(?) p.(His101Tyr) g.8997440G>A Copied from the Exome Variant Server FAM9B_000022 86/10563 84/6728 2/3835
?/? c.330A>G r.(=) p.(=) g.8997411T>C Copied from the Exome Variant Server FAM9B_000021 1/10563 0/6728 1/3835
?/? c.345C>T r.(=) p.(=) g.8997396G>A Copied from the Exome Variant Server FAM9B_000020 2/10562 1/6728 1/3834
?/? c.369_371del r.(?) p.(Glu124del) g.8997370_8997372del Copied from the Exome Variant Server FAM9B_000019 126/10205 95/6484 31/3721
?/? c.391A>G r.(?) p.(Ile131Val) g.8997350T>C Copied from the Exome Variant Server FAM9B_000018 2/10561 0/6728 2/3833
?/? c.394-49G>A r.(=) p.(=) g.8996056C>T Copied from the Exome Variant Server FAM9B_000017 13/10551 13/6721 0/3830
?/? c.394-43A>C r.(=) p.(=) g.8996050T>G Copied from the Exome Variant Server FAM9B_000016 3/10555 2/6725 1/3830
?/? c.394-27_394-26insT r.(=) p.(=) g.8996033_8996034insA Copied from the Exome Variant Server FAM9B_000015 2/10200 0/6483 2/3717
?/? c.396A>G r.(=) p.(=) g.8996005T>C Copied from the Exome Variant Server FAM9B_000014 1/10563 0/6728 1/3835
?/? c.432T>C r.(=) p.(=) g.8995969A>G Copied from the Exome Variant Server FAM9B_000013 2/10563 2/6728 0/3835
?/? c.476G>A r.(?) p.(Arg159His) g.8995925C>T Copied from the Exome Variant Server FAM9B_000012 1/10563 1/6728 0/3835
?/? c.486C>T r.(=) p.(=) g.8995915G>A Copied from the Exome Variant Server FAM9B_000011 3/10563 0/6728 3/3835
?/? c.487G>A r.(?) p.(Val163Ile) g.8995914C>T Copied from the Exome Variant Server FAM9B_000010 1/10563 1/6728 0/3835
?/? c.492+10A>G r.(=) p.(=) g.8995899T>C Copied from the Exome Variant Server FAM9B_000009 23/10563 20/6728 3/3835
?/? c.492+44G>A r.(=) p.(=) g.8995865C>T Copied from the Exome Variant Server FAM9B_000008 2/10558 1/6723 1/3835
?/? c.492+48A>T r.(=) p.(=) g.8995861T>A Copied from the Exome Variant Server FAM9B_000007 10/10558 0/6723 10/3835
?/? c.493-47G>A r.(=) p.(=) g.8993671C>T Copied from the Exome Variant Server FAM9B_000006 180/10558 166/6727 14/3831
?/? c.493-19A>C r.(=) p.(=) g.8993643T>G Copied from the Exome Variant Server FAM9B_000005 3/10562 3/6727 0/3835
?/? c.494C>T r.(?) p.(Ala165Val) g.8993623G>A Copied from the Exome Variant Server FAM9B_000004 1/10561 0/6726 1/3835
?/? c.521A>G r.(?) p.(Asp174Gly) g.8993596T>C Copied from the Exome Variant Server FAM9B_000003 2/10562 2/6727 0/3835
?/? c.534C>T r.(=) p.(=) g.8993583G>A Copied from the Exome Variant Server FAM9B_000002 2/10562 0/6727 2/3835
?/? c.*31+6T>C r.(=) p.(=) g.8993519A>G Copied from the Exome Variant Server FAM9B_000001 3/10556 3/6725 0/3831
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