Transcript #00025889 (NM_000245.2, MET gene)

Transcript name met proto-oncogene, transcript variant 2
Gene name MET (met proto-oncogene (hepatocyte growth factor receptor))
Chromosome 7
Transcript - NCBI ID NM_000245.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_000236.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2023-12-07 11:27:15 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-207C>G r.(?) p.(=)
-/. - c.-14-4G>A r.spl? p.?
-/. - c.-14-4G>A r.spl? p.?
-?/. - c.36C>T r.(?) p.(Leu12=)
-?/. - c.71G>A r.(?) p.(Gly24Glu)
-/. - c.103A>T r.(?) p.(Met35Leu)
-?/. - c.110T>C r.(?) p.(Val37Ala)
-?/. - c.110T>C r.(?) p.(Val37Ala)
-/. - c.144G>A r.(?) p.(Ala48=)
-?/. - c.144G>A r.(=) p.(=)
-/. - c.144G>A r.(?) p.(Ala48=)
-/. - c.144G>A r.(?) p.(Ala48=)
?/. - c.244G>A r.(?) p.(Ala82Thr)
?/. - c.387A>T r.(?) p.(Gln129His)
-/. - c.390C>T r.(?) p.(Leu130=)
-/. - c.390C>T r.(?) p.(Leu130=)
-/. - c.390C>T r.(?) p.(Leu130=)
-?/. - c.406G>A r.(?) p.(Val136Ile)
?/. - c.467C>T r.(?) p.(Ser156Leu)
-?/. - c.467C>T r.(?) p.(Ser156Leu)
?/. - c.467C>T r.(?) p.(Ser156Leu)
-?/. - c.467C>T r.(?) p.(Ser156Leu)
-/. - c.504G>T r.(?) p.(Glu168Asp)
-?/. - c.504G>T r.(?) p.(Glu168Asp)
-/. - c.504G>T r.(?) p.(Glu168Asp)
-?/. - c.504G>T r.(?) p.(Glu168Asp)
-/. - c.504G>T r.(?) p.(Glu168Asp)
-/. - c.534C>T r.(?) p.(Ser178=)
-/. - c.534C>T r.(?) p.(Ser178=)
-/. - c.534C>T r.(?) p.(Ser178=)
-?/. - c.607T>A r.(?) p.(Ser203Thr)
-?/. - c.607T>A r.(?) p.(Ser203Thr)
?/. - c.611_613del r.(?) p.(Ser204del)
?/. - c.665C>T r.(?) p.(Thr222Met)
-?/. - c.789G>A r.(?) p.(Thr263=)
-?/. - c.798G>A r.(?) p.(Arg266=)
-?/. - c.798G>A r.(?) p.(Arg266=)
-?/. - c.833T>A r.(?) p.(Ile278Lys)
?/. - c.883C>T r.(?) p.(Pro295Ser)
?/. - c.889G>C r.(?) p.(Glu297Gln)
?/. - c.901A>G r.(?) p.(Thr301Ala)
?/. - c.901A>G r.(?) p.(Thr301Ala)
-?/. - c.901A>G r.(?) p.(Thr301Ala)
?/. - c.938T>C r.(?) p.(Val313Ala)
-/. - c.948A>G r.(?) p.(Ile316Met)
-?/. - c.948A>G r.(?) p.(Ile316Met)
?/. - c.959C>T r.(?) p.(Ala320Val)
?/. - c.1039G>A r.(?) p.(Ala347Thr)
?/. - c.1039G>A r.(?) p.(Ala347Thr)
-/. - c.1039G>A r.(?) p.(Ala347Thr)
-?/. - c.1039G>A r.(?) p.(Ala347Thr)
-/. - c.1085T>C r.(?) p.(Met362Thr)
-?/. - c.1085T>C r.(?) p.(Met362Thr)
-/. - c.1085T>C r.(?) p.(Met362Thr)
-?/. - c.1101C>A r.(?) p.(Ile367=)
-/. - c.1124A>G r.(?) p.(Asn375Ser)
-/. - c.1124A>G r.(?) p.(Asn375Ser)
-/. - c.1124A>G r.(?) p.(Asn375Ser)
-/. - c.1131C>T r.(?) p.(Ile377=)
-/. - c.1131C>T r.(?) p.(Ile377=)
?/. - c.1171G>A r.(?) p.(Gly391Arg)
-?/. - c.1201-15del r.(=) p.(=)
?/. - c.1285T>A r.(?) p.(Leu429Ile)
-?/. - c.1393-6G>A r.(=) p.(=)
-/. - c.1393-6G>A r.(=) p.(=)
-?/. - c.1393-6G>A r.(=) p.(=)
-?/. - c.1414C>T r.(?) p.(Pro472Ser)
-?/. - c.1451A>G r.(?) p.(His484Arg)
-?/. - c.1528-131G>T r.(?) p.(?)
-?/. - c.1584A>G r.(?) p.(=)
-?/. - c.1659C>T r.(?) p.(Ser553=)
-/. - c.1701+58del r.(=) p.(=)
?/. - c.1733G>C r.(?) p.(Gly578Ala)
-/. - c.1944A>G r.(?) p.(Gln648=)
-/. - c.1944A>G r.(?) p.(Gln648=)
-?/. - c.1966-36A>G r.(=) p.(=)
-?/. - c.1966-23T>C r.(=) p.(=)
-?/. - c.1966-17T>C r.(=) p.(=)
-?/. - c.2103-4T>C r.spl? p.?
?/. - c.2110A>G r.(?) p.(Asn704Asp)
?/. - c.2198C>T r.(?) p.(Thr733Ile)
?/. - c.2254T>G r.(?) p.(Ser752Ala)
-/. - c.2264+89C>T r.(=) p.(=)
-?/. - c.2265-38C>T r.(=) p.(=)
-?/. - c.2318C>T r.(?) p.(Pro773Leu)
-?/. - c.2318C>T r.(?) p.(Pro773Leu)
?/. - c.2543T>C r.(?) p.(Val848Ala)
-?/. - c.2584-23T>A r.(=) p.(=)
-/. - c.2584-9del r.(=) p.(=)
-/. - c.2584-9del r.(=) p.(=)
-/. - c.2584-9del r.(=) p.(=)
-/. - c.2584-9del r.(=) p.(=)
-/. - c.2584-9dup r.(=) p.(=)
-?/. - c.2584-8_2584-7del r.(=) p.(=)
-?/. - c.2584-7C>T r.(=) p.(=)
-?/. - c.2584-7del r.(=) p.(=)
-?/. - c.2584-7del r.(=) p.(=)
-?/. - c.2584-6_2584-4dup r.spl? p.?
-?/. - c.2584-4_2584-3insTTTTT r.spl? p.?
-?/. - c.2584-4_2584-3insTTTTTT r.spl? p.?
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