Transcript #00000080

Transcript name Fanconi anemia, complementation group G
Gene name FANCG (FA complementation group G)
Chromosome 9
Transcript - NCBI ID NM_004629.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_004620.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

74 entries on 1 page. Showing entries 1 - 74.
Legend  

Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.20C>T r.(?) p.(Ser7Phe)
./. - c.65G>A r.(?) p.(Arg22Gln)
./. - c.76C>T r.(?) p.(Gln26*)
./. - c.77A>G r.(?) p.(Gln26Arg)
./. - c.77A>G r.(?) p.(Gln26Arg)
./. - c.85-18C>T r.(=) p.(=)
./. - c.308-11A>G r.(=) p.(=)
./. - c.421C>T r.(?) p.(Arg141Cys)
./. - c.421C>T r.(?) p.(Arg141Cys)
./. - c.486A>T r.(?) p.(Leu162Phe)
./. - c.646+12A>G r.(=) p.(=)
./. - c.647-16C>A r.(=) p.(=)
./. - c.647-16C>A r.(=) p.(=)
./. - c.819G>A r.(=) p.(=)
./. - c.924+31G>A r.(=) p.(=)
./. - c.924+31G>A r.(=) p.(=)
./. - c.925-50A>C r.(=) p.(=)
./. - c.925-23C>A r.(=) p.(=)
./. - c.955C>A r.(?) p.(Pro319Thr)
./. - c.1076+36C>T r.(=) p.(=)
./. - c.1076+36C>T r.(=) p.(=)
./. - c.1120T>C r.(=) p.(=)
./. - c.1192T>C r.(=) p.(=)
./. - c.1192T>C r.(=) p.(=)
./. - c.1260G>C r.(?) p.(Leu420Phe)
./. - c.1297C>T r.(?) p.(Arg433Trp)
./. - c.1367A>T r.(?) p.(His456Leu)
./. - c.1367A>T r.(?) p.(His456Leu)
./. - c.1367A>T r.(?) p.(His456Leu)
./. - c.1367A>T r.(?) p.(His456Leu)
./. - c.1367A>T r.(?) p.(His456Leu)
./. - c.1480+40T>C r.(=) p.(=)
./. - c.1481-36G>A r.(=) p.(=)
./. - c.1481-23T>C r.(=) p.(=)
./. - c.1492A>C r.(?) p.(Asn498His)
./. - c.1492A>C r.(?) p.(Asn498His)
./. - c.1492A>C r.(?) p.(Asn498His)
./. - c.1498G>A r.(?) p.(Glu500Lys)
./. - c.1498G>A r.(?) p.(Glu500Lys)
./. - c.1498G>A r.(?) p.(Glu500Lys)
./. - c.1544C>T r.(?) p.(Ala515Val)
./. - c.1545C>T r.(=) p.(=)
./. - c.1614C>A r.(=) p.(=)
./. - c.1637-27A>G r.(=) p.(=)
./. - c.1637-24C>G r.(=) p.(=)
./. - c.1637-24_1637-23del r.(=) p.(=)
./. - c.1638T>C r.(=) p.(=)
./. - c.1700C>T r.(?) p.(Ala567Val)
./. - c.1761-44C>T r.(=) p.(=)
./. - c.1761-28C>A r.(=) p.(=)
./. - c.1761-28C>A r.(=) p.(=)
./. - c.1761-28C>A r.(=) p.(=)
./. - c.1761-28C>A r.(=) p.(=)
./. - c.1761G>T r.(?) p.(Trp587Cys)
./. - c.1801C>T r.(?) p.(Arg601Cys)
./. - c.1814G>A r.(?) p.(Arg605His)
Legend