Transcript #00002512 (NM_032217.3, ANKRD17 gene)

Transcript name transcript variant 1
Gene name ANKRD17 (ankyrin repeat domain 17)
Chromosome 4
Transcript - NCBI ID NM_032217.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_115593.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

59 entries on 1 page. Showing entries 1 - 59.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.58C>T r.(?) p.(Pro20Ser)
?/. - c.90dup r.(?) p.(Ala31ArgfsTer47)
?/. - c.244C>T r.(?) p.(Pro82Ser)
-?/. - c.372_374dup r.(?) p.(Asp124dup)
-?/. - c.393+35258A>G r.(=) p.(=)
-?/. - c.615A>G r.(?) p.(Thr205=)
-?/. - c.705-5A>C r.spl? p.?
+?/. - c.718G>C r.(?) p.(Glu240Gln)
?/. - c.994T>G r.(?) p.(Ser332Ala)
?/. - c.1238A>C r.(?) p.(His413Pro)
-/. - c.1870-7dup r.(=) p.(=)
?/. - c.1999G>A r.(?) p.(Val667Ile)
?/. - c.2086-3T>C r.spl? p.?
?/. - c.2162A>G r.(?) p.(Asn721Ser)
?/. - c.2210C>A r.(?) p.(Pro737Gln)
?/. - c.2229+1G>A r.spl? p.?
?/. - c.2390G>C r.(?) p.(Gly797Ala)
+/. - c.2644C>T r.(?) p.(Gln882*)
?/. - c.2750_2755del r.(?) p.(Val917_Gly918del)
?/. - c.2782C>T r.(?) p.(Arg928Trp)
-?/. - c.2876C>A r.(?) p.(Pro959His)
-?/. - c.3131G>C r.(?) p.(Ser1044Thr)
?/. - c.3301A>G r.(?) p.(Thr1101Ala)
?/. - c.3359T>G r.(?) p.(Leu1120Arg)
+?/. 21 c.3962del r.(?) p.(Asp1321Valfs*4)
?/. - c.4019T>C r.(?) p.(Ile1340Thr)
?/. - c.4103T>G r.(?) p.(Val1368Gly)
?/. - c.4118T>C r.(?) p.(Val1373Ala)
+/. - c.4229_4232del r.(?) p.(Asn1410Serfs*9)
?/. - c.4341_4344del r.(?) p.(Gln1448LeufsTer12)
?/. - c.4939G>T r.(?) p.(Val1647Leu)
?/. - c.5135G>A r.(?) p.(Arg1712His)
+?/. - c.5304_5310del r.(?) p.(Asp1770Ter)
-?/. - c.5327+371A>T r.(=) p.(=)
-?/. - c.5398A>T r.(?) p.(Ile1800Phe)
?/. - c.5411T>C r.(?) p.(Ile1804Thr)
?/. - c.5638T>C r.(?) p.(Ser1880Pro)
?/. - c.5857A>T r.(?) p.(Asn1953Tyr)
?/. - c.6377C>G r.(?) p.(Ser2126Cys)
-?/. - c.6412C>G r.(?) p.(Pro2138Ala)
?/. - c.6493G>A r.(?) p.(Gly2165Arg)
?/. - c.6554C>T r.(?) p.(Thr2185Ile)
?/. - c.6575C>T r.(?) p.(Ser2192Leu)
-?/. - c.6811G>A r.(?) p.(Gly2271Arg)
-?/. - c.6838C>A r.(?) p.(Pro2280Thr)
-?/. - c.6962-247_6962-246insC r.(=) p.(=)
-?/. - c.7170A>G r.(?) p.(Ala2390=)
+?/. 31 c.7214C>A r.(?) p.(Ser2405*)
?/. - c.7375A>C r.(?) p.(Ile2459Leu)
?/. - c.7409-1G>T r.spl? p.?
-?/. - c.7505G>A r.(?) p.(Arg2502Gln)
-?/. - c.7552G>A r.(?) p.(Val2518Ile)
-?/. - c.7618A>G r.(?) p.(Met2540Val)
-?/. - c.7729A>C r.(?) p.(Thr2577Pro)
-?/. - c.7729A>G r.(?) p.(Thr2577Ala)
?/. - c.7736A>G r.(?) p.(Asn2579Ser)
-?/. - c.7765C>G r.(?) p.(Pro2589Ala)
?/. - c.7772C>G r.(?) p.(Ala2591Gly)
-?/. - c.*6887A>C r.(=) p.(=)
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