Transcript #00018301 (NM_173630.3, RTTN gene)

Transcript name rotatin
Gene name RTTN (rotatin)
Chromosome 18
Transcript - NCBI ID NM_173630.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_775901.3
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

179 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-10142286_*19308723del r.0? p.0?
-/. - c.-19T>G r.(?) p.(=)
?/. - c.19A>G r.(?) p.(Ile7Val)
+/. - c.31+1G>T r.spl? p.?
-?/. - c.31+18C>T r.(=) p.(=)
-/. - c.32-3C>T r.spl? p.?
-?/. - c.71G>C r.(?) p.(Ser24Thr)
?/. - c.80G>A r.(?) p.(Cys27Tyr)
?/. - c.98T>C r.(?) p.(Leu33Ser)
-/. - c.153A>G r.(?) p.(Glu51=)
-/. - c.183G>A r.(?) p.(Lys61=)
-/. - c.220-12T>C r.(=) p.(=)
+?/. - c.278T>C r.(?) p.(Leu93Pro)
-?/. - c.282G>T r.(?) p.(Arg94=)
?/. - c.301C>A r.(?) p.(Leu101Met)
?/. - c.343C>T r.(?) p.(Leu115Phe)
-/. - c.376T>G r.(?) p.(Ser126Ala)
?/. - c.455T>G r.(?) p.(Phe152Cys)
-?/. - c.455T>G r.(?) p.(Phe152Cys)
+/. - c.460C>T r.(?) p.(Gln154Ter)
-?/. - c.488-15C>T r.(=) p.(=)
+?/. - c.494A>C r.(?) p.(Gln165Pro)
-?/. - c.561C>A r.(?) p.(Val187=)
-/. - c.578+15G>A r.(=) p.(=)
?/. - c.590G>A r.(?) p.(Ser197Asn)
?/. - c.601A>T r.(?) p.(Thr201Ser)
-?/. - c.602C>G r.(?) p.(Thr201Ser)
?/. - c.630G>C r.(?) p.(Leu210Phe)
?/. - c.635A>C r.(?) p.(Asp212Ala)
-/. - c.694-19C>T r.(=) p.(=)
-/. - c.694-9T>G r.(=) p.(=)
-?/. - c.708G>T r.(?) p.(Leu236=)
-/. - c.725_727dup r.(?) p.(Gly242dup)
-/. - c.725_727dup r.(?) p.(Gly242dup)
-/. - c.734A>G r.(?) p.(Lys245Arg)
-/. - c.734A>G r.(?) p.(Lys245Arg)
-/. - c.734A>G r.(?) p.(Lys245Arg)
?/. - c.803A>G r.(?) p.(Asn268Ser)
-?/. - c.805T>C r.(?) p.(Phe269Leu)
-/. - c.841+26C>T r.(=) p.(=)
-/. - c.842-30A>G r.(=) p.(=)
-?/. - c.885A>G r.(?) p.(Ala295=)
-?/. - c.905A>C r.(?) p.(Gln302Pro)
?/. - c.905A>C r.(?) p.(Gln302Pro)
-?/. - c.905A>C r.(?) p.(Gln302Pro)
?/. - c.952C>T r.(?) p.(Arg318Cys)
-?/. - c.1008-4G>T r.spl? p.?
-/. - c.1008-4G>T r.spl? p.?
?/. - c.1305G>C r.(?) p.(Met435Ile)
-?/. - c.1306-16G>A r.(=) p.(=)
-?/. - c.1330G>A r.(?) p.(Gly444Arg)
-?/. - c.1423A>G r.(?) p.(Ser475Gly)
-/. - c.1458G>A r.(?) p.(Thr486=)
-?/. - c.1563T>C r.(?) p.(Ile521=)
?/. - c.1654T>C r.(?) p.(Cys552Arg)
-/. - c.1665C>A r.(?) p.(Asn555Lys)
-?/. - c.1665C>A r.(?) p.(Asn555Lys)
-/. - c.1665C>A r.(?) p.(Asn555Lys)
?/. - c.1665C>A r.(?) p.(Asn555Lys)
-/. - c.1802+29G>A r.(=) p.(=)
?/. - c.1832T>C r.(?) p.(Leu611Pro)
-?/. - c.1842A>G r.(?) p.(Glu614=)
-?/. - c.1921A>G r.(?) p.(Ile641Val)
-?/. - c.1929+3G>A r.spl? p.?
?/. - c.1963G>A r.(?) p.(Val655Met)
?/. - c.2030T>G r.(?) p.(Phe677Cys)
-/. - c.2055+7C>T r.(=) p.(=)
-/. - c.2055+7C>T r.(=) p.(=)
+?/. - c.2056-2A>G r.spl? p.?
-/. - c.2172+18C>A r.(=) p.(=)
?/. - c.2183A>C r.(?) p.(Asp728Ala)
-?/. - c.2237A>C r.(?) p.(Asp746Ala)
?/. - c.2255C>T r.(?) p.(Pro752Leu)
-?/. - c.2298G>A r.(?) p.(Val766=)
-/. - c.2309+12G>A r.(=) p.(=)
-?/. - c.2340A>T r.(?) p.(Ala780=)
?/. - c.2377C>T r.(?) p.(Arg793Cys)
-/. - c.2482-10del r.(=) p.(=)
-?/. - c.2581+8C>T r.(=) p.(=)
?/. - c.2582-1G>A r.spl? p.?
+?/. 18 c.2594A>G r.(?) p.(His865Arg)
+?/. 18 c.2594A>G r.(?) p.(His865Arg)
+?/. 20 c.2594A>G r.(?) p.(His865Arg)
-?/. - c.2610G>A r.(?) p.(Lys870=)
-?/. - c.2680T>C r.(?) p.(Cys894Arg)
+/. - c.2796A>T r.(?) p.(Leu932Phe)
+?/. - c.2796A>T r.(?) p.(Leu932Phe)
?/. - c.2804A>G r.(?) p.(His935Arg)
?/. - c.2804A>G r.(?) p.(His935Arg)
?/. - c.2804A>G r.(?) p.(His935Arg)
-?/. - c.2821G>C r.(?) p.(Val941Leu)
-?/. - c.2821G>C r.(?) p.(Val941Leu)
-/. - c.2856A>G r.(=) p.(=)
-?/. - c.2856A>G r.(?) p.(Leu952=)
-/. - c.2886-9A>G r.(=) p.(=)
-/. - c.2886-9A>G r.(=) p.(=)
+/. - c.2953A>G r.(?) p.(Arg985Gly)
-?/. - c.3048G>A r.(?) p.(Pro1016=)
?/. - c.3167C>T r.(?) p.(Ser1056Phe)
-?/. - c.3235A>G r.(?) p.(Ile1079Val)
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