Transcript #00001621 (NM_032608.5, MYO18B gene)

Transcript name myosin XVIIIB
Gene name MYO18B (myosin XVIIIB)
Chromosome 22
Transcript - NCBI ID NM_032608.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_115997.5
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2012-09-13 13:42:46 +02:00 (CEST)
Date last edited N/A


Variants

83 entries on 1 page. Showing entries 1 - 83.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-109-3C>T r.spl? p.?
?/. - c.20T>G r.(?) p.(Leu7Arg)
?/. - c.22G>A r.(?) p.(Ala8Thr)
./. - c.31G>T r.(?) p.(Glu11*)
+?/. - c.193C>T r.(?) p.(Arg65*)
?/. - c.199-5C>G r.spl? p.?
-?/. - c.309C>G r.(?) p.(Asp103Glu)
-?/. - c.637G>A r.(?) p.(Ala213Thr)
-?/. - c.936A>G r.(?) p.(Gln312=)
-?/. - c.1512+9G>C r.(=) p.(=)
-?/. - c.1513-3C>T r.spl? p.?
+?/. - c.1537G>C r.(?) p.(Ala513Pro)
?/. - c.1551G>C r.(?) p.(Trp517Cys)
?/. - c.1589T>C r.(?) p.(Leu530Pro)
?/. - c.1641G>C r.(?) p.(Trp547Cys)
?/. - c.1811C>G r.(?) p.(Thr604Arg)
?/. - c.2098C>T r.(?) p.(Leu700Phe)
?/. - c.2101C>T r.(?) p.(Arg701Trp)
-?/. - c.2315C>T r.(?) p.(Thr772Met)
-?/. - c.2377-4G>A r.spl? p.?
-?/. - c.2377-4G>A r.spl? p.?
?/. - c.2596C>A r.(?) p.(Leu866Met)
+/. - c.2662C>T r.(?) p.(Arg888Ter)
-?/. - c.2695+4C>G r.spl? p.?
?/. - c.2738C>T r.(?) p.(Ser913Leu)
?/. - c.2860C>A r.(?) p.(His954Asn)
-?/. - c.2869A>G r.(?) p.(Lys957Glu)
-?/. - c.2879C>T r.(?) p.(Ala960Val)
-?/. - c.2966A>G r.(?) p.(Gln989Arg)
?/. - c.3034G>T r.(?) p.(Ala1012Ser)
-?/. - c.3209-4C>T r.spl? p.?
?/. - c.3220C>A r.(?) p.(Leu1074Met)
-?/. - c.3291C>A r.(?) p.(Asp1097Glu)
?/. - c.3291C>A r.(?) p.(Asp1097Glu)
?/. - c.3431C>T r.(?) p.(Ala1144Val)
+?/. - c.3775+1G>C r.spl? p.?
?/. - c.3811C>T r.(?) p.(Arg1271Trp)
?/. - c.3968G>T r.(?) p.(Gly1323Val)
-?/. - c.4021G>A r.(?) p.(Val1341Ile)
?/. - c.4273C>T r.(?) p.(Arg1425Trp)
-?/. - c.4330T>A r.(?) p.(Ser1444Thr)
-?/. - c.4544-3C>T r.spl? p.?
-?/. - c.4566C>T r.(?) p.(=)
?/. - c.4708A>G r.(?) p.(Met1570Val)
?/. - c.5058G>T r.(?) p.(Leu1686Phe)
?/. - c.5206C>T r.(?) p.(Arg1736Cys)
?/. - c.5239C>T r.(?) p.(Arg1747Cys)
-?/. - c.5364+8G>A r.(=) p.(=)
-/. - c.5749-11del r.(=) p.(=)
-?/. - c.5854A>G r.(?) p.(Ile1952Val)
?/. - c.5878G>A r.(?) p.(Val1960Met)
-?/. - c.5885G>A r.(?) p.(Arg1962Gln)
?/. - c.5909C>T r.(?) p.(Ala1970Val)
?/. - c.5984G>A r.(?) p.(Arg1995Gln)
?/. - c.6100G>A r.(?) p.(Asp2034Asn)
?/. - c.6122G>A r.(?) p.(Arg2041Gln)
-?/. - c.6140G>A r.(?) p.(Arg2047Gln)
?/. - c.6223C>T r.(?) p.(Arg2075Trp)
-?/. - c.6226C>T r.(?) p.(Arg2076Trp)
?/. - c.6244G>T r.(?) p.(Ala2082Ser)
-?/. - c.6297G>A r.(?) p.(=)
?/. - c.6333G>A r.(?) p.(Met2111Ile)
-?/. - c.6507G>T r.(?) p.(Gln2169His)
-?/. - c.6593G>A r.(?) p.(Arg2198His)
-?/. - c.6596G>A r.(?) p.(Arg2199Gln)
-?/. - c.6716C>G r.(?) p.(Ser2239Trp)
?/. - c.6752C>G r.(?) p.(Ser2251Trp)
?/. - c.6772C>T r.(?) p.(Arg2258Trp)
?/. - c.6838A>C r.(?) p.(Ile2280Leu)
?/. - c.6856G>T r.(?) p.(Ala2286Ser)
-?/. - c.6885C>T r.(?) p.(Gly2295=)
?/. - c.6986T>C r.(?) p.(Ile2329Thr)
?/. - c.7078A>C r.(?) p.(Ser2360Arg)
-?/. - c.7147C>T r.(?) p.(Arg2383Trp)
-?/. - c.7147C>T r.(?) p.(Arg2383Trp)
-/. - c.7221G>A r.(?) p.(Gln2407=)
-?/. - c.7221G>A r.(?) p.(Gln2407=)
-?/. - c.7345C>T r.(?) p.(Arg2449Trp)
-?/. - c.7345C>T r.(?) p.(Arg2449Trp)
?/. - c.7345C>T r.(?) p.(Arg2449Trp)
-?/. - c.7506C>T r.(?) p.(=)
-?/. - c.7537G>A r.(?) p.(Gly2513Ser)
-?/. - c.7595G>A r.(?) p.(Arg2532Gln)
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