Transcript #00021056

Transcript name wingless-type MMTV integration site family, member 10A
Gene name WNT10A (wingless-type MMTV integration site family, member 10A)
Chromosome 2
Transcript - NCBI ID NM_025216.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_079492.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

69 entries on 1 page. Showing entries 1 - 69.
Legend  

Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.85C>T r.(=) p.(=)
?/? c.125A>G r.(?) p.(Asn42Ser)
?/? c.143G>A r.(?) p.(Arg48His)
?/? c.149C>T r.(?) p.(Pro50Leu)
?/? c.152C>G r.(?) p.(Pro51Arg)
?/? c.159C>T r.(=) p.(=)
?/? c.160G>A r.(?) p.(Val54Met)
?/? c.172del r.(?) p.(Asn58Thrfs*5)
?/? c.203G>A r.(?) p.(Ser68Asn)
?/? c.208C>T r.(?) p.(Arg70Trp)
?/? c.212A>T r.(?) p.(Gln71Leu)
?/? c.216G>T r.(?) p.(Met72Ile)
?/? c.319T>A r.(?) p.(Cys107Ser)
?/? c.321C>A r.(?) p.(Cys107*)
?/? c.337C>T r.(?) p.(Arg113Cys)
?/? c.349C>T r.(?) p.(Pro117Ser)
?/? c.357G>A r.(=) p.(=)
?/? c.376+13C>T r.(=) p.(=)
?/? c.377-49G>A r.(=) p.(=)
?/? c.377-42A>C r.(=) p.(=)
?/? c.377-38C>T r.(=) p.(=)
?/? c.377-11T>C r.(=) p.(=)
?/? c.383G>A r.(?) p.(Arg128Gln)
?/? c.388A>G r.(?) p.(Ser130Gly)
?/? c.391G>A r.(?) p.(Ala131Thr)
?/? c.408C>G r.(?) p.(Ile136Met)
?/? c.420C>T r.(=) p.(=)
?/? c.427C>T r.(?) p.(His143Tyr)
?/? c.441T>C r.(=) p.(=)
?/? c.443C>T r.(?) p.(Ala148Val)
?/? c.444G>A r.(=) p.(=)
?/? c.460C>A r.(?) p.(Leu154Met)
?/? c.466G>T r.(?) p.(Ala156Ser)
?/? c.480T>C r.(=) p.(=)
?/? c.483G>C r.(=) p.(=)
?/? c.487C>T r.(?) p.(Arg163Trp)
?/? c.488G>A r.(?) p.(Arg163Gln)
?/? c.491G>A r.(?) p.(Arg164Gln)
?/? c.493G>A r.(?) p.(Gly165Arg)
?/? c.498C>T r.(=) p.(=)
?/? c.499G>A r.(?) p.(Glu167Lys)
?/? c.511C>T r.(?) p.(Arg171Cys)
?/? c.514A>T r.(?) p.(Arg172Trp)
?/? c.529T>C r.(=) p.(=)
?/? c.551G>A r.(?) p.(Arg184His)
?/? c.558G>A r.(=) p.(=)
?/? c.561C>T r.(=) p.(=)
?/? c.579G>A r.(=) p.(=)
?/? c.591C>T r.(=) p.(=)
?/? c.594G>A r.(=) p.(=)
?/? c.630G>C r.(?) p.(Glu210Asp)
?/? c.637G>A r.(?) p.(Gly213Ser)
?/? c.649G>A r.(?) p.(Asp217Asn)
?/? c.652A>G r.(?) p.(Met218Val)
?/? c.662G>T r.(?) p.(Gly221Val)
?/? c.664G>T r.(?) p.(Glu222*)
?/? c.667C>T r.(?) p.(Arg223Cys)
?/? c.668G>A r.(?) p.(Arg223His)
?/? c.682T>A r.(?) p.(Phe228Ile)
?/? c.712A>G r.(?) p.(Ile238Val)
?/? c.719C>T r.(?) p.(Ala240Val)
?/? c.725T>C r.(?) p.(Met242Thr)
?/? c.737A>G r.(?) p.(Asn246Ser)
?/? c.756+14C>T r.(=) p.(=)
?/? c.756+20G>A r.(=) p.(=)
?/? c.757-17G>T r.(=) p.(=)
?/? c.817C>A r.(?) p.(Leu273Ile)
?/? c.1057G>C r.(?) p.(Asp353His)
?/? c.1087A>C r.(?) p.(Asn363His)
Legend