Transcript #00015042

Transcript name oligodendrocyte myelin glycoprotein
Gene name OMG (oligodendrocyte myelin glycoprotein)
Chromosome 17
Transcript - NCBI ID NM_002544.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_002535.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

1434 entries on 15 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
-/. - c.-81780A>G benign r.(?) p.(=)
?/. - c.-77035T>C VUS r.(?) p.(=)
?/. - c.-77028T>C VUS r.(?) p.(=)
?/. - c.-77001C>T VUS r.(?) p.(=)
-?/. - c.-76985A>G likely benign r.(?) p.(=)
-?/. - c.-76937G>A likely benign r.(?) p.(=)
-?/. - c.-76931G>A likely benign r.(?) p.(=)
-/. - c.-76894G>A benign r.(?) p.(=)
?/. - c.-70128T>C VUS r.(?) p.(=)
-/. - c.-63721_-63718dup benign r.(?) p.(=)
-/. - c.-63684_-63682del benign r.(?) p.(=)
-/. - c.-63574T>C benign r.(?) p.(=)
-?/. - c.-63544C>T likely benign r.(?) p.(=)
-?/. - c.-63540G>A likely benign r.(?) p.(=)
?/. - c.-63508G>T VUS r.(?) p.(=)
?/. - c.-63404G>C VUS r.(?) p.(=)
-?/. - c.-63367A>T likely benign r.(?) p.(=)
+/. - c.-63337C>T pathogenic r.(?) p.(=)
-?/. - c.-63335G>A likely benign r.(?) p.(=)
+/. - c.-61863del pathogenic r.(?) p.(=)
+/. - c.-61861_-61858del pathogenic r.(?) p.(=)
-?/. - c.-61857C>T likely benign r.(?) p.(=)
+/. - c.-61818T>A pathogenic r.(?) p.(=)
-?/. - c.-61790C>T likely benign r.(?) p.(=)
-/. - c.-61494del benign r.(?) p.(=)
-/. - c.-61493C>T benign r.(?) p.(=)
-/. - c.-61493C>T benign r.(?) p.(=)
+/. - c.-61471del pathogenic r.(?) p.(=)
+/. - c.-61466del pathogenic r.(?) p.(=)
-?/. - c.-61457T>C likely benign r.(?) p.(=)
+/. - c.-61433dup pathogenic r.(?) p.(=)
+/. - c.-61430G>T pathogenic r.(?) p.(=)
-/. - c.-61421A>G benign r.(?) p.(=)
+/. - c.-61421_-61420del pathogenic r.(?) p.(=)
+/. - c.-61418_-61417del pathogenic r.(?) p.(=)
+/. - c.-61416G>A pathogenic r.(?) p.(=)
+/. - c.-61393A>T pathogenic r.(?) p.(=)
+/. - c.-61360_-61358delinsTT pathogenic r.(?) p.(=)
-?/. - c.-61357T>C likely benign r.(?) p.(=)
+/. - c.-61349dup pathogenic r.(?) p.(=)
+/. - c.-61332del pathogenic r.(?) p.(=)
-?/. - c.-61331C>A likely benign r.(?) p.(=)
-?/. - c.-61330C>A likely benign r.(?) p.(=)
-?/. - c.-61329T>A likely benign r.(?) p.(=)
?/. - c.-61328A>C VUS r.(?) p.(=)
-?/. - c.-61324G>A likely benign r.(?) p.(=)
-?/. - c.-61315del likely benign r.(?) p.(=)
-/. - c.-61315del benign r.(?) p.(=)
+/. - c.-61314G>C pathogenic r.(?) p.(=)
-/. - c.-61312C>A benign r.(?) p.(=)
-/. - c.-61312C>A benign r.(?) p.(=)
-/. - c.-61307G>A benign r.(?) p.(=)
-/. - c.-60250G>T benign r.(?) p.(=)
?/. - c.-60223T>G VUS r.(?) p.(=)
+/. - c.-60221C>T pathogenic r.(?) p.(=)
+/. - c.-60217del pathogenic r.(?) p.(=)
+/. - c.-60204del pathogenic r.(?) p.(=)
+/. - c.-60204dup pathogenic r.(?) p.(=)
+/. - c.-60198del pathogenic r.(?) p.(=)
+/. - c.-60191del pathogenic r.(?) p.(=)
?/. - c.-60180C>G VUS r.(?) p.(=)
-/. - c.-60160C>T benign r.(?) p.(=)
+/. - c.-60159G>A pathogenic r.(?) p.(=)
+/. - c.-60145T>C pathogenic r.(?) p.(=)
-/. - c.-60128C>T benign r.(?) p.(=)
-?/. - c.-60122A>T likely benign r.(?) p.(=)
+/. - c.-60119C>T pathogenic r.(?) p.(=)
+/. - c.-60118T>C pathogenic r.(?) p.(=)
-/. - c.-60102dup benign r.(?) p.(=)
-/. - c.-59963C>T benign r.(?) p.(=)
+?/. - c.-59944T>A likely pathogenic r.(?) p.(=)
+/. - c.-59933dup pathogenic r.(?) p.(=)
+/. - c.-59918G>A pathogenic r.(?) p.(=)
+/. - c.-59917_-59904del pathogenic r.(?) p.(=)
+/. - c.-59894dup pathogenic r.(?) p.(=)
+/. - c.-59886A>T pathogenic r.(?) p.(=)
+/. - c.-59875del pathogenic r.(?) p.(=)
+/. - c.-59870C>A pathogenic r.(?) p.(=)
+/. - c.-59864del pathogenic r.(?) p.(=)
+/. - c.-59862G>T pathogenic r.(?) p.(=)
+/. - c.-59855T>A pathogenic r.(?) p.(=)
+/. - c.-59850A>C pathogenic r.(?) p.(=)
?/. - c.-59839C>G VUS r.(?) p.(=)
-/. - c.-59836T>C benign r.(?) p.(=)
+/. - c.-59834G>A pathogenic r.(?) p.(=)
-/. - c.-59827G>A benign r.(?) p.(=)
-/. - c.-59827G>A benign r.(?) p.(=)
+/. - c.-59816G>A pathogenic r.(?) p.(=)
-/. - c.-59788C>T benign r.(?) p.(=)
+/. - c.-59421_-59420del pathogenic r.(?) p.(=)
-/. - c.-59396G>T benign r.(?) p.(=)
+/. - c.-59391del pathogenic r.(?) p.(=)
+/. - c.-59362del pathogenic r.(?) p.(=)
+/. - c.-59358del pathogenic r.(?) p.(=)
-?/. - c.-59318C>T likely benign r.(?) p.(=)
-/. - c.-59318C>T benign r.(?) p.(=)
-?/. - c.-59318C>T likely benign r.(?) p.(=)
-?/. - c.-59314G>T likely benign r.(?) p.(=)
-?/. - c.-55245G>A likely benign r.(?) p.(=)
-?/. - c.-55234T>C likely benign r.(?) p.(=)
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