All transcript variants in gene NTF4

Information The variants shown are described using the NM_006179.4 transcript reference sequence.

29 entries on 1 page. Showing entries 1 - 29.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.203G>A r.(?) p.(Arg68Gln) g.49565052C>T Copied from the Exome Variant Server NTF4_000029 37/12092 2/8048 35/4044
?/? c.243G>A r.(=) p.(=) g.49565012C>T Copied from the Exome Variant Server NTF4_000028 1/12828 0/8492 1/4336
?/? c.260C>A r.(?) p.(Pro87Gln) g.49564995G>T Copied from the Exome Variant Server NTF4_000027 1/12870 0/8526 1/4344
?/? c.263C>T r.(?) p.(Ala88Val) g.49564992G>A Copied from the Exome Variant Server NTF4_000026 29/12872 27/8526 2/4346
?/? c.266G>A r.(?) p.(Ser89Asn) g.49564989C>T Copied from the Exome Variant Server NTF4_000025 1/12870 1/8528 0/4342
?/? c.277G>A r.(?) p.(Glu93Lys) g.49564978C>T Copied from the Exome Variant Server NTF4_000024 1/12894 0/8536 1/4358
?/? c.320G>C r.(?) p.(Arg107Pro) g.49564935C>G Copied from the Exome Variant Server NTF4_000023 1/12966 1/8572 0/4394
?/? c.327C>T r.(=) p.(=) g.49564928G>A Copied from the Exome Variant Server NTF4_000022 1/12978 0/8582 1/4396
?/? c.331G>C r.(?) p.(Val111Leu) g.49564924C>G Copied from the Exome Variant Server NTF4_000020 1/12994 1/8594 0/4400
?/? c.340C>G r.(?) p.(Arg114Gly) g.49564915G>C Copied from the Exome Variant Server NTF4_000018 2/12998 2/8594 0/4404
?/? c.366C>T r.(=) p.(=) g.49564889G>A Copied from the Exome Variant Server NTF4_000021 2/12988 1/8588 1/4400
?/? c.379G>T r.(?) p.(Ala127Ser) g.49564876C>A Copied from the Exome Variant Server NTF4_000019 1/12946 0/8566 1/4380
?/? c.380C>T r.(?) p.(Ala127Val) g.49564875G>A Copied from the Exome Variant Server NTF4_000017 1/12946 0/8566 1/4380
?/? c.397C>T r.(?) p.(Arg133Cys) g.49564858G>A Copied from the Exome Variant Server NTF4_000016 1/13002 0/8598 1/4404
?/? c.418C>T r.(?) p.(Arg140Cys) g.49564837G>A Copied from the Exome Variant Server NTF4_000015 1/13006 0/8600 1/4406
?/? c.436G>T r.(?) p.(Ala146Ser) g.49564819C>A Copied from the Exome Variant Server NTF4_000014 1/13006 0/8600 1/4406
?/? c.481G>A r.(?) p.(Val161Met) g.49564774C>T Copied from the Exome Variant Server NTF4_000013 1/13006 1/8600 0/4406
?/? c.493C>A r.(?) p.(His165Asn) g.49564762G>T Copied from the Exome Variant Server NTF4_000012 1/13006 1/8600 0/4406
?/? c.517A>T r.(?) p.(Lys173*) g.49564738T>A Copied from the Exome Variant Server NTF4_000011 1/13006 0/8600 1/4406
?/? c.527A>G r.(?) p.(Tyr176Cys) g.49564728T>C Copied from the Exome Variant Server NTF4_000010 1/13006 1/8600 0/4406
?/? c.532C>T r.(?) p.(Arg178Trp) g.49564723G>A Copied from the Exome Variant Server NTF4_000009 1/13002 1/8596 0/4406
?/? c.552C>G r.(=) p.(=) g.49564703G>C Copied from the Exome Variant Server NTF4_000008 1/13006 1/8600 0/4406
?/? c.559C>T r.(?) p.(Arg187Cys) g.49564696G>A Copied from the Exome Variant Server NTF4_000007 1/13006 0/8600 1/4406
?/? c.565G>C r.(?) p.(Gly189Arg) g.49564690C>G Copied from the Exome Variant Server NTF4_000006 2/13006 2/8600 0/4406
?/? c.580C>T r.(?) p.(Arg194*) g.49564675G>A Copied from the Exome Variant Server NTF4_000005 1/13006 1/8600 0/4406
?/? c.603C>T r.(=) p.(=) g.49564652G>A Copied from the Exome Variant Server NTF4_000004 1/13004 0/8600 1/4404
?/? c.605C>T r.(?) p.(Thr202Ile) g.49564650G>A Copied from the Exome Variant Server NTF4_000003 1/13004 1/8600 0/4404
?/? c.616C>T r.(?) p.(Arg206Trp) g.49564639G>A Copied from the Exome Variant Server NTF4_000002 9/13004 8/8598 1/4406
?/? c.620C>T r.(?) p.(Thr207Ile) g.49564635G>A Copied from the Exome Variant Server NTF4_000001 1/12998 1/8596 0/4402
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