Transcript #00000081 (NM_001127500.1, MET gene)

Transcript name met proto-oncogene (hepatocyte growth factor receptor)
Gene name MET (met proto-oncogene (hepatocyte growth factor receptor))
Chromosome 7
Transcript - NCBI ID NM_001127500.1
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. 01 c.-187-u529A>C - -
./. 01 c.-187-u20C>G - -
./. 02 c.36dup - p.Val13ArgfsX15
./. 02 c.134A>G - p.Asn45Ser
./. 02 c.143C>T - p.Ala48Val
./. 02 c.144G>A - p.Ala48Ala
./. 02 c.287del - p.Phe96SerfsX25
./. 02 c.334del - p.Trp112GlyfsX9
./. 02 c.428G>A - p.Arg143Gln
./. 02 c.467C>T - p.Ser156Leu
./. 02 c.485del - p.Phe162SerfsX5
./. 02 c.504G>T - p.Glu168Asp
./. 02 c.620dup - p.Asp208ArgfsX29
./. 02 c.632T>G - p.Leu211Trp
./. 02 c.713T>C - p.Leu238Ser
./. 02 c.716C>G - p.Pro239Arg
./. 02 c.822del - p.His275ThrfsX4
./. 02 c.925A>C - p.Thr309Pro
./. 02 c.948A>G - p.Ile316Met
./. 02 c.959C>T - p.Ala320Val
./. 02 c.959C>T - p.Ala320Val
./. 02 c.1023del - p.Leu342PhefsX42
./. 02 c.1029_1030insT - p.Gly344TrpfsX52
./. 02 c.1035dup - p.Phe346ValfsX50
./. 02 c.1085T>C - p.Met362Thr
./. 02 c.1124A>G - p.Asn375Ser
./. 02 c.1124A>G - p.Asn375Ser
./. 02 c.1142A>C - p.Asn381Thr
./. 03 c.1204C>A - p.Leu402Ile
./. 03 c.1214delA - p.Asn405IlefsX35
./. 04 c.1484C>T - p.Thr495Ile
./. 05 c.1676A>G - p.Gln559Arg
./. 06 c.1771C>T - p.Arg591Trp
./. 07 c.1898A>T - p.His633Leu
./. 07 c.1931A>G - p.His644Arg
./. 07 c.1944A>G - p.Gln648Gln
./. 07 c.1944A>G - p.Gln648Gln
./. 07 c.1946A>G - p.Tyr649Cys
./. 08 c.1983T>A - p.Ser661Arg
./. 09 c.2192G>A - p.Arg731Gln
./. 09 c.2215C>T - p.Arg739Cys
./. 09 c.2216G>A - p.Arg739His
./. 09 c.2239A>G - p.Ile747Val
./. 09 c.2352_2353insA - p.Leu785ThrfsX5
./. 10 c.2356A>G - p.Asn786Asp
./. 10 c.2372C>T - p.Pro791Leu
./. 11 c.2431C>T - p.Arg811Cys
./. 11 c.2556T>G - p.Ile852Met
./. 11 c.2586dup - p.Glu863X
./. 11 c.2611G>T - p.Gly871Cys
./. 13 c.2821_2822insA - p.Val941AspfsX40
./. 13 c.2851G>A - p.Gly951Arg
./. 14 c.2962C>T - p.Arg988Cys
./. 14 c.2962C>T - p.Arg988Cys
./. 14 c.2962C>T - p.Arg988Cys
./. 14 c.2963G>A - p.Arg988His
./. 14 c.2997T>G - p.Asp999Glu
./. 14 c.2999G>T - p.Arg1000Met
./. 14 c.3025C>T - p.Pro1009Ser
./. 14 c.3029C>T - p.Thr1010Ile
./. 14 c.3029C>T - p.Thr1010Ile
./. 14 c.3075del - p.Pro1026GlnfsX21
./. 15 c.3119G>A - p.Arg1040Gln
./. 15 c.3145A>G - p.Met1049Val
./. 15 c.3192_3193insT - p.Leu1065SerfsX8
./. 15 c.3212T>C - p.Ile1071Thr
./. 15 c.3214_3215insT - p.Asp1072ValfsX22
./. 15 c.3253C>A - p.Gln1085Lys
./. 16 c.3328G>A - p.Val1110Ile
./. 16 c.3328G>A - p.Val1110Ile
./. 16 c.3328G>A - p.Val1110Ile
./. 16 c.3334C>T - p.His1112Tyr
./. 16 c.3335A>G - p.His1112Arg
./. 16 c.3335A>G - p.His1112Arg
./. 16 c.3335A>G - p.His1112Arg
./. 16 c.3335A>T - p.His1112Leu
./. 16 c.3341C>G - p.Thr1114Ser
./. 16 c.3343T>G - p.Leu1115Val
./. 16 c.3370C>G - p.His1124Asp
./. 16 c.3370C>G - p.His1124Asp
./. 17 c.3410G>T - p.Gly1137Val
./. 17 c.3446T>C - p.Met1149Thr
./. 17 c.3446T>C - p.Met1149Thr
./. 17 c.3446T>C - p.Met1149Thr
./. 17 c.3497G>A - p.Arg1166Gln
./. 18 c.3592G>A - p.Asp1198Asn
./. 18 c.3616G>C - p.Val1206Leu
./. 18 c.3616G>C - p.Val1206Leu
./. 18 c.3616G>T - p.Val1206Leu
./. 18 c.3619delG - p.Ala1207Profs
./. 18 c.3637C>G - p.Leu1213Val
./. 18 c.3637C>G - p.Lys1213Val
./. 19 c.3712G>A - p.Val1238Ile
./. 19 c.3712G>A - p.Val1238Ile
./. 19 c.3736G>A - p.Asp1246Asn
./. 19 c.3736G>A - p.Asp1246Asn
./. 19 c.3736G>C - p.Asp1246His
./. 19 c.3736G>C - p.Asp1246His
./. 19 c.3742T>C - p.Tyr1248His
./. 19 c.3742T>C - p.Tyr1248His
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