All transcript variants in gene GSPT2

Information The variants shown are described using the NM_018094.4 transcript reference sequence.

26 entries on 1 page. Showing entries 1 - 26.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.-6G>T r.(=) p.(=) g.51486717G>T Copied from the Exome Variant Server GSPT2_000001 1/10481 0/6670 1/3811
?/? c.11_13del r.(?) p.(Ser8del) g.51486733_51486735del Copied from the Exome Variant Server GSPT2_000002 100/10109 67/6420 33/3689
?/? c.68C>T r.(?) p.(Pro23Leu) g.51486790C>T Copied from the Exome Variant Server GSPT2_000003 111/10553 2/6721 109/3832
?/? c.91G>A r.(?) p.(Gly31Arg) g.51486813G>A Copied from the Exome Variant Server GSPT2_000004 1/10559 0/6725 1/3834
?/? c.95T>A r.(?) p.(Val32Asp) g.51486817T>A Copied from the Exome Variant Server GSPT2_000005 1/10558 1/6726 0/3832
?/? c.229A>T r.(?) p.(Thr77Ser) g.51486951A>T Copied from the Exome Variant Server GSPT2_000006 2/10561 0/6727 2/3834
?/? c.252C>T r.(=) p.(=) g.51486974C>T Copied from the Exome Variant Server GSPT2_000007 3/10546 2/6717 1/3829
?/? c.353T>C r.(?) p.(Leu118Ser) g.51487075T>C Copied from the Exome Variant Server GSPT2_000008 1/10558 0/6724 1/3834
?/? c.404C>T r.(?) p.(Pro135Leu) g.51487126C>T Copied from the Exome Variant Server GSPT2_000009 1/10560 1/6726 0/3834
?/? c.423G>A r.(=) p.(=) g.51487145G>A Copied from the Exome Variant Server GSPT2_000010 151/10562 3/6728 148/3834
?/? c.512C>A r.(?) p.(Pro171His) g.51487234C>A Copied from the Exome Variant Server GSPT2_000011 1/10556 0/6725 1/3831
?/? c.515C>G r.(?) p.(Pro172Arg) g.51487237C>G Copied from the Exome Variant Server GSPT2_000012 1/10554 1/6725 0/3829
?/? c.580G>T r.(?) p.(Val194Leu) g.51487302G>T Copied from the Exome Variant Server GSPT2_000013 1/10562 1/6727 0/3835
?/? c.625A>G r.(?) p.(Ile209Val) g.51487347A>G Copied from the Exome Variant Server GSPT2_000014 1/10562 0/6728 1/3834
?/? c.722A>C r.(?) p.(Glu241Ala) g.51487444A>C Copied from the Exome Variant Server GSPT2_000015 1/10563 1/6728 0/3835
?/? c.862G>A r.(?) p.(Ala288Thr) g.51487584G>A Copied from the Exome Variant Server GSPT2_000016 1/10563 1/6728 0/3835
?/? c.889A>G r.(?) p.(Asn297Asp) g.51487611A>G Copied from the Exome Variant Server GSPT2_000017 1/10563 1/6728 0/3835
?/? c.919T>C r.(=) p.(=) g.51487641T>C Copied from the Exome Variant Server GSPT2_000018 84/10563 0/6728 84/3835
?/? c.1182C>T r.(=) p.(=) g.51487904C>T Copied from the Exome Variant Server GSPT2_000020 1/10563 0/6728 1/3835
?/? c.1236A>G r.(=) p.(=) g.51487958A>G Copied from the Exome Variant Server GSPT2_000021 1/10563 1/6728 0/3835
?/? c.1274G>T r.(?) p.(Arg425Ile) g.51487996G>T Copied from the Exome Variant Server GSPT2_000022 1/10563 0/6728 1/3835
?/? c.1303A>G r.(?) p.(Ile435Val) g.51488025A>G Copied from the Exome Variant Server GSPT2_000023 1/10563 1/6728 0/3835
?/? c.1461A>T r.(=) p.(=) g.51488183A>T Copied from the Exome Variant Server GSPT2_000024 13/10563 0/6728 13/3835
?/? c.1599C>T r.(=) p.(=) g.51488321C>T Copied from the Exome Variant Server GSPT2_000025 1/10563 1/6728 0/3835
?/? c.1864A>C r.(?) p.(Lys622Gln) g.51488586A>C Copied from the Exome Variant Server GSPT2_000026 1/10563 1/6728 0/3835
?/? c.*48C>T r.(=) p.(=) g.51488657C>T Copied from the Exome Variant Server GSPT2_000019 20/10409 0/6660 20/3749
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