Transcript #00017498

Transcript name transcript variant 4
Gene name SLC37A4 (solute carrier family 37 (glucose-6-phosphate transporter), member 4)
Chromosome 11
Transcript - NCBI ID NM_001467.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_001458.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

95 entries on 1 page. Showing entries 1 - 95.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-42G>C r.(=) p.(=)
?/? c.21C>G r.(=) p.(=)
?/? c.112T>C r.(=) p.(=)
?/? c.141T>G r.(?) p.(Asp47Glu)
?/? c.148+25T>C r.(=) p.(=)
?/? c.149-38C>G r.(=) p.(=)
?/? c.149-16G>A r.(=) p.(=)
?/? c.149-14A>G r.(=) p.(=)
?/? c.170C>T r.(?) p.(Ser57Leu)
?/? c.174A>G r.(=) p.(=)
?/? c.183T>C r.(=) p.(=)
?/? c.192G>A r.(=) p.(=)
?/? c.201T>C r.(=) p.(=)
?/? c.204G>A r.(=) p.(=)
?/? c.205G>T r.(?) p.(Val69Leu)
?/? c.230G>A r.(?) p.(Arg77His)
?/? c.242C>T r.(?) p.(Ser81Phe)
?/? c.292T>G r.(?) p.(Ser98Ala)
?/? c.299T>C r.(?) p.(Val100Ala)
?/? c.345_346insGG r.(?) p.(Leu116Glyfs*31)
?/? c.377G>A r.(?) p.(Arg126Gln)
?/? c.382-44T>C r.(=) p.(=)
?/? c.382-23A>G r.(=) p.(=)
?/? c.405C>T r.(=) p.(=)
?/? c.467C>T r.(?) p.(Ala156Val)
?/? c.492C>A r.(?) p.(Ser164Arg)
?/? c.496C>T r.(?) p.(Arg166Cys)
?/? c.497G>A r.(?) p.(Arg166His)
?/? c.522A>C r.(=) p.(=)
?/? c.540C>G r.(=) p.(=)
?/? c.541C>T N/A N/A
?/? c.568T>C N/A N/A
?/? c.591G>A N/A N/A
?/? c.594A>T N/A N/A
?/? c.604C>T N/A N/A
?/? c.606T>G N/A N/A
?/? c.626+14C>T r.(=) p.(=)
?/? c.626+19C>T r.(=) p.(=)
?/? c.627-51G>A r.(=) p.(=)
?/? c.627-44G>A r.(=) p.(=)
?/? c.627-23G>A r.(=) p.(=)
?/? c.629T>C N/A N/A
?/? c.664G>A N/A N/A
?/? c.732C>T N/A N/A
?/? c.785+3A>G r.spl? p.?
?/? c.785+6A>T r.(=) p.(=)
?/? c.785+43A>T r.(=) p.(=)
?/? c.786-33C>G r.(=) p.(=)
?/? c.812G>T N/A N/A
?/? c.847C>T r.(=) p.(=)
?/? c.850G>A N/A N/A
?/? c.871+6C>T r.(=) p.(=)
?/? c.871+17G>T r.(=) p.(=)
?/? c.871+50C>T r.(=) p.(=)
?/? c.871+51G>A r.(=) p.(=)
?/? c.871+56G>A r.(=) p.(=)
?/? c.872-28C>T r.(=) p.(=)
?/? c.872-27G>A r.(=) p.(=)
?/? c.872-21T>C r.(=) p.(=)
?/? c.873C>T N/A N/A
?/? c.907C>A r.(?) p.(Leu303Met)
?/? c.931C>T N/A N/A
?/? c.956C>T N/A N/A
?/? c.969C>T r.(=) p.(=)
?/? c.985+24C>T r.(=) p.(=)
?/? c.985+25G>A r.(=) p.(=)
?/? c.985+31G>A r.(=) p.(=)
?/? c.985+34C>T r.(=) p.(=)
?/? c.985+166_985+168del r.(=) p.(=)
?/? c.985+228C>G r.(=) p.(=)
?/? c.985+247C>T r.(=) p.(=)
?/? c.985+248G>A r.(=) p.(=)
?/? c.986-48C>T r.(=) p.(=)
?/? c.986-32C>T r.(=) p.(=)
?/? c.986-30C>G r.(=) p.(=)
?/? c.986-18C>T r.(=) p.(=)
?/? c.992A>G N/A N/A
?/? c.1013T>C r.(?) p.(Phe338Ser)
?/? c.1016G>T r.(?) p.(Gly339Val)
?/? c.1026C>T N/A N/A
?/? c.1043_1044del r.(?) p.(Phe349Trpfs*52)
?/? c.1048T>C N/A N/A
?/? c.1063C>T N/A N/A
?/? c.1104T>C r.(=) p.(=)
?/? c.1124+8T>C r.(=) p.(=)
?/? c.1125-7_1125-6del r.(=) p.(=)
?/? c.1169C>T N/A N/A
?/? c.1202del r.(?) p.(Val402*)
?/? c.1225G>A r.(?) p.(Ala409Thr)
?/? c.1253C>T N/A N/A
?/? c.1276C>T N/A N/A
?/? c.1279G>A N/A N/A
?/? c.1287A>C N/A N/A
?/? c.*5A>C r.(=) p.(=)
?/? c.*7T>G r.(=) p.(=)
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