Transcript #00008978

Transcript name keratin 27
Gene name KRT27 (keratin 27)
Chromosome 17
Transcript - NCBI ID NM_181537.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_853515.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

93 entries on 1 page. Showing entries 1 - 93.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-32C>T r.(=) p.(=)
?/? c.-19G>T r.(=) p.(=)
?/? c.-15C>T r.(=) p.(=)
?/? c.-14A>G r.(=) p.(=)
?/? c.-11C>T r.(=) p.(=)
?/? c.-7G>A r.(=) p.(=)
?/? c.-5A>G r.(=) p.(=)
?/? c.10C>T r.(?) p.(Arg4Cys)
?/? c.46G>A r.(?) p.(Gly16Arg)
?/? c.60T>C r.(=) p.(=)
?/? c.75T>C r.(=) p.(=)
?/? c.155G>C r.(?) p.(Ser52Thr)
?/? c.178G>A r.(?) p.(Gly60Arg)
?/? c.189C>T r.(=) p.(=)
?/? c.190G>A r.(?) p.(Gly64Arg)
?/? c.232G>C r.(?) p.(Gly78Arg)
?/? c.257T>G r.(?) p.(Val86Gly)
?/? c.276C>T r.(=) p.(=)
?/? c.307C>T r.(?) p.(Arg103*)
?/? c.319G>A r.(?) p.(Glu107Lys)
?/? c.327C>T r.(=) p.(=)
?/? c.328G>A r.(?) p.(Ala110Thr)
?/? c.386G>A r.(?) p.(Arg129His)
?/? c.400G>T r.(?) p.(Asp134Tyr)
?/? c.429C>G r.(?) p.(Asp143Glu)
?/? c.430G>A r.(?) p.(Glu144Lys)
?/? c.444+17C>T r.(=) p.(=)
?/? c.445-1G>C r.spl? p.?
?/? c.496G>A r.(?) p.(Ala166Thr)
?/? c.502C>T r.(=) p.(=)
?/? c.527+33del r.(=) p.(=)
?/? c.527+33dup r.(=) p.(=)
?/? c.528-27G>A r.(=) p.(=)
?/? c.529T>C r.(?) p.(Phe177Leu)
?/? c.571A>C r.(?) p.(Ile191Leu)
?/? c.575A>G r.(?) p.(Asn192Ser)
?/? c.577G>A r.(?) p.(Gly193Ser)
?/? c.593T>C r.(?) p.(Leu198Pro)
?/? c.649G>A r.(?) p.(Glu217Lys)
?/? c.677A>G r.(?) p.(His226Arg)
?/? c.684+31T>A r.(=) p.(=)
?/? c.684+34C>G r.(=) p.(=)
?/? c.684+49T>G r.(=) p.(=)
?/? c.685-8T>C r.(=) p.(=)
?/? c.706G>A r.(?) p.(Ala236Thr)
?/? c.709G>A r.(?) p.(Ala237Thr)
?/? c.745C>G r.(?) p.(Pro249Ala)
?/? c.754G>T r.(?) p.(Asp252Tyr)
?/? c.784G>A r.(?) p.(Ala262Thr)
?/? c.801C>T r.(=) p.(=)
?/? c.818G>A r.(?) p.(Arg273Lys)
?/? c.825G>A r.(=) p.(=)
?/? c.840C>G r.(?) p.(Asn280Lys)
?/? c.846+6_846+7insA r.(=) p.(=)
?/? c.846+13T>A r.(=) p.(=)
?/? c.846+23C>T r.(=) p.(=)
?/? c.846+35T>C r.(=) p.(=)
?/? c.847-35_847-34insG r.(=) p.(=)
?/? c.847-27G>A r.(=) p.(=)
?/? c.847-20C>G r.(=) p.(=)
?/? c.847-7G>A r.(=) p.(=)
?/? c.847-6T>A r.(=) p.(=)
?/? c.850G>A r.(?) p.(Ala284Thr)
?/? c.882T>A r.(=) p.(=)
?/? c.885C>G r.(=) p.(=)
?/? c.914T>C r.(?) p.(Ile305Thr)
?/? c.931C>T r.(?) p.(Leu311Phe)
?/? c.960C>A r.(=) p.(=)
?/? c.964T>A r.(?) p.(Leu322Ile)
?/? c.972+4A>C r.spl? p.?
?/? c.972+19A>C r.(=) p.(=)
?/? c.972+49_972+50insA r.(=) p.(=)
?/? c.973-39G>A r.(=) p.(=)
?/? c.1005C>T r.(=) p.(=)
?/? c.1054G>T r.(?) p.(Ala352Ser)
?/? c.1086C>A r.(=) p.(=)
?/? c.1093G>A r.(?) p.(Glu365Lys)
?/? c.1108G>C r.(?) p.(Glu370Gln)
?/? c.1160C>T r.(?) p.(Thr387Ile)
?/? c.1190+13G>A r.(=) p.(=)
?/? c.1190+44A>G r.(=) p.(=)
?/? c.1191-41T>C r.(=) p.(=)
?/? c.1191-18C>T r.(=) p.(=)
?/? c.1191-11T>C r.(=) p.(=)
?/? c.1201A>C r.(?) p.(Lys401Gln)
?/? c.1214A>G r.(?) p.(Tyr405Cys)
?/? c.1241-33_1241-31del r.(=) p.(=)
?/? c.1243T>G r.(?) p.(Ser415Ala)
?/? c.1292G>A r.(?) p.(Arg431His)
?/? c.1340C>T r.(?) p.(Thr447Ile)
?/? c.1364A>G r.(?) p.(Gln455Arg)
?/? c.1369G>A r.(?) p.(Val457Met)
?/? c.*12_*13insT r.(=) p.(=)
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