Transcript #00014783 (NM_005654.4, NR2F1 gene)

Transcript name nuclear receptor subfamily 2, group F, member 1
Gene name NR2F1 (nuclear receptor subfamily 2, group F, member 1)
Chromosome 5
Transcript - NCBI ID NM_005654.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_005645.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -


Variants

117 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.-506041_*1935315del r.0 p.0
+/. - c.-325733_*639854del r.0 p.0
+?/. _1_3_ c.-1687_*240{0} r.0 p.0
+?/. _1_3_ c.-1687_*240{0} r.0 p.0
+?/. _1_3_ c.-1687_*240{0} r.0 p.0
+?/. _1_3_ c.-1687_*240{0} r.0 p.0
+?/. _1_3_ c.-1687_*240{0} r.0 p.0
+?/. _1_3_ c.-1687_*240{0} r.0 p.0
+?/. _1_3_ c.-1687_*240{0} r.0 p.0
+/. _1_3_ c.-1687_*240{0} r.0 p.0
+/. _1_3_ c.-1687_*240{0} r.0 p.0
+/. - c.1A>G r.0 p.0
+/. - c.2T>C r.0 p.0
+/. - c.2T>C r.0 p.0
+/. - c.2T>C r.0 p.0
+/. - c.2T>C r.0 p.0
+/. - c.2T>G r.0 p.0
+/. - c.2T>G r.0 p.0
+/. - c.2_4delinsGGA r.0 p.0
?/. - c.49G>C r.(?) p.(Gly17Arg)
+?/. - c.51_69dup r.(?) p.(Asn24Glyfs*379)
?/. - c.73C>G r.(?) p.(Pro25Ala)
+?/. - c.78_96del r.(?) p.(Gln28Alafs*85)
+?/. - c.82C>T r.(?) p.(Gln28*)
+?/. - c.103_113delinsCGCCGCCGC r.(?) p.(Gly35Argfs*361)
?/. - c.107G>C r.(?) p.(Gly36Ala)
+?/. - c.115G>T r.(?) p.(Glu39*)
+?/. - c.192del r.(?) p.(Gly65Alafs*54)
-?/. - c.237G>C r.(?) p.(Gln79His)
+?/. - c.237G>C r.(?) p.(Gln79His)
+?/. - c.237G>C r.(?) p.(Gln79His)
?/. - c.253G>T r.(?) p.(Glu85*)
+?/. - c.256T>C r.(?) p.(Cys86Arg)
+?/. - c.257G>T r.(?) p.(Cys86Phe)
+?/. - c.262G>A r.(?) p.(Val88Met)
+?/. - c.284G>T r.(?) p.(Gly95Val)
?/. - c.284G>T r.(?) p.(Gly95Val)
+/. - c.286A>G r.(?) p.(Lys96Glu)
+?/. - c.289C>T r.(?) p.(His97Tyr)
+?/. - c.289C>T r.(?) p.(His97Tyr)
+?/. - c.290A>C r.(?) p.(His97Pro)
+?/. - c.291del r.(?) p.(Tyr98Thrfs*21)
+?/. - c.292T>C r.(?) p.(Tyr98His)
+?/. - c.293A>G r.(?) p.(Tyr98Cys)
+?/. - c.311A>G r.(?) p.(Glu104Gly)
+/. - c.313G>A r.(?) p.(Gly105Ser)
+?/. - c.313G>A r.(?) p.(Gly105Ser)
+/. - c.314G>A r.(?) p.(Gly105Asp)
+/. - c.314G>A r.(?) p.(Gly105Asp)
+/. - c.319A>G r.(?) p.(Lys107Glu)
?/. - c.320A>G r.(?) p.(Lys107Arg)
+?/. - c.323G>A r.(?) p.(Ser108Asn)
+?/. - c.323G>A r.(?) p.(Ser108Asn)
?/. - c.323G>C r.(?) p.(Ser108Thr)
+?/. - c.323G>T r.(?) p.(Ser108Ile)
+?/. - c.328_330del r.(?) p.(Phe110del)
+?/. - c.328_330del r.(?) p.(Phe110del)
+/. 1 c.335G>A r.(?) p.(Arg112Lys)
+/. 1 c.339C>A r.(?) p.(Ser113Arg)
+/. - c.339C>A r.(?) p.(Ser113Arg)
+/. 1 c.344G>C r.(?) p.(Arg115Pro)
+?/. - c.365G>C r.(?) p.(Cys122Ser)
+?/. - c.366C>G r.(?) p.(Cys122Trp)
+?/. - c.368G>T r.(?) p.(Arg123Leu)
+?/. - c.380dup r.(?) p.(Asn127Lysfs*270)
+?/. - c.382T>C r.(?) p.(Cys128Arg)
+?/. - c.403C>A r.(?) p.(Arg135Ser)
+?/. - c.403C>T r.(?) p.(Arg135Cys)
+?/. - c.403C>T r.(?) p.(Arg135Cys)
+/. 1 c.413G>A r.(?) p.(Cys138Tyr)
+?/. - c.413G>A r.(?) p.(Cys138Tyr)
+?/. - c.417A>T r.(?) p.(Gln139His)
+?/. - c.425G>A r.(?) p.(Arg142His)
+?/. - c.425G>T r.(?) p.(Arg142Leu)
+?/. - c.436T>C r.(?) p.(Cys146Arg)
+?/. - c.436T>C r.(?) p.(Cys146Arg)
?/. - c.452T>C r.(?) p.(Met151Thr)
+?/. - c.463G>A r.(?) p.(Ala155Thr)
+?/. - c.463G>A r.(?) p.(Ala155Thr)
+/. - c.513C>A r.(?) p.(Tyr171*)
+?/. - c.513C>G r.(?) p.(Tyr171*)
+/. - c.535dup r.(?) p.(Leu179Profs*218)
?/. - c.581G>T r.(?) p.(Arg194Leu)
+/. - c.602C>A r.(?) p.(Ser201*)
+/. - c.603_606del r.(?) p.(Arg202Thrfs*154)
-?/. - c.708C>T r.(?) p.(Asn236=)
+?/. - c.729_730delinsCT r.(?) p.(Gln244*)
+/. 2 c.755T>C r.(?) p.(Leu252Pro)
+/. 2 c.854C>A r.(?) p.(Ser285*)
?/. - c.883T>C r.(?) p.(Phe295Leu)
?/. 2 c.909G>C r.(?) p.(Gln303His)
+?/. - c.931G>C r.(?) p.(Ala311Pro)
+/. - c.954G>C r.(?) p.(Glu318Asp)
+?/. - c.954G>C r.(?) p.(Glu318Asp)
+?/. 2 c.965T>A r.(?) p.(Leu322His)
+?/. - c.968A>C r.(?) p.(Lys323Thr)
+?/. - c.968_969del r.(?) p.(Lys323Serfs*73)
-/. - c.991+19G>A r.(=) p.(=)
-?/. - c.1016C>T r.(?) p.(Ala339Val)
+?/. - c.1024G>A r.(?) p.(Glu342Lys)
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