Transcript #00004931 (NM_017424.2, CECR1 gene)

Transcript name transcript variant 1
Gene name CECR1 (cat eye syndrome chromosome region, candidate 1)
Chromosome 22
Transcript - NCBI ID NM_017424.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_059120.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

88 entries on 1 page. Showing entries 1 - 88.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-12107del r.(?) p.(=)
-/. - c.-9717G>A r.(?) p.(=)
-/. - c.138G>C r.(?) p.(=)
-?/. - c.138G>C r.(?) p.(=)
+/. - c.139G>A r.(?) p.(Gly47Arg)
+/. - c.139G>A r.(?) p.(Gly47Arg)
+?/. - c.140G>A r.(?) p.(Gly47Glu)
+/. - c.140G>T r.(?) p.(Gly47Val)
+/. - c.140G>T r.(?) p.(Gly47Val)
+/. - c.140G>T r.(?) p.(Gly47Val)
+/. - c.140G>T r.(?) p.(Gly47Val)
+/. - c.140G>T r.(?) p.(Gly47Val)
+/. - c.144del r.(?) p.(Arg49Glyfs*4)
+/. - c.145del r.(?) p.(Arg49Glyfs*4)
+/. - c.158del r.(?) p.(Asn53IlefsTer12)
-/. - c.159= r.(=) p.(Asn53=)
-/. - c.159= r.(=) p.(Asn53=)
-/. - c.159= r.(=) p.(Asn53=)
-?/. - c.194C>T r.(?) p.(Thr65Met)
?/. - c.229A>C r.(?) p.(Thr77Pro)
?/. - c.244C>T r.(?) p.(Pro82Ser)
?/. - c.272A>G r.(?) p.(His91Arg)
-?/. - c.362T>C r.(?) p.(Met121Thr)
+?/. - c.385A>C r.(?) p.(Thr129Pro)
+/. - c.506G>A r.(?) p.(Arg169Gln)
+/. - c.506G>A r.(?) p.(Arg169Gln)
+/. - c.506G>A r.(?) p.(Arg169Gln)
+/. - c.506G>A r.(?) p.(Arg169Gln)
+/. - c.506G>A r.(?) p.(Arg169Gln)
-?/. - c.508A>G r.(?) p.(Lys170Glu)
-?/. - c.511C>T r.(?) p.(Arg171Trp)
?/. - c.562C>G r.(?) p.(Leu188Val)
+?/. - c.578C>T r.(?) p.(Pro193Leu)
-?/. - c.689G>A r.(?) p.(Arg230Gln)
-?/. - c.702G>A r.(?) p.(Glu234=)
?/. - c.707A>G r.(?) p.(Tyr236Cys)
+?/. - c.753G>A r.(?) p.(=)
-?/. - c.783C>T r.(?) p.(Asp261=)
-?/. - c.882-17C>T r.(=) p.(=)
-?/. - c.882-11del r.(=) p.(=)
-?/. - c.927G>A r.(?) p.(Met309Ile)
-?/. - c.927G>A r.(?) p.(Met309Ile)
?/. - c.927G>A r.(?) p.(Met309Ile)
+/. - c.932T>G r.(?) p.(Leu311Arg)
-?/. - c.950C>T r.(?) p.(Thr317Met)
-?/. - c.950C>T r.(?) p.(Thr317Met)
+/. - c.973-2A>G r.spl? p.?
+/. - c.973-2A>G r.spl? p.?
+?/. - c.973-2A>G r.spl? p.?
-/. - c.1004A>G r.(?) p.(His335Arg)
-/. - c.1004A>G r.(?) p.(His335Arg)
-/. - c.1004A>G r.(?) p.(His335Arg)
-?/. - c.1045G>A r.(?) p.(Val349Ile)
-?/. - c.1045G>A r.(?) p.(Val349Ile)
-?/. - c.1045G>A r.(?) p.(Val349Ile)
?/. - c.1055C>G r.(?) p.(Pro352Arg)
+?/. - c.1069G>A r.(?) p.(Ala357Thr)
+/. - c.1072G>A r.(?) p.(Gly358Arg)
+/. - c.1072G>A r.(?) p.(Gly358Arg)
-?/. - c.1081+3G>A r.spl? p.?
-?/. - c.1081+11G>A r.(=) p.(=)
-?/. - c.1081+18G>A r.(=) p.(=)
-/. - c.1081+87T>C r.(=) p.(=)
-?/. - c.1082-42_1082-16del r.(=) p.(=)
+/. - c.1196G>A r.(?) p.(Trp399*)
-/. - c.1240-5C>G r.spl? p.?
-/. - c.1240-5C>G r.spl? p.?
-/. - c.1240-5C>G r.spl? p.?
?/. - c.1252G>T r.(?) p.(Val418Leu)
+/. - c.1334T>A r.(?) p.(Met445Lys)
+/. - c.1358A>G r.(?) p.(Tyr453Cys)
-/. - c.1359T>C r.(?) p.(Tyr453=)
-/. - c.1359T>C r.(?) p.(Tyr453=)
-/. - c.1359T>C r.(?) p.(Tyr453=)
+/. - c.1367A>G r.(?) p.(Tyr456Cys)
?/. - c.1379T>A r.(?) p.(Met460Lys)
?/. - c.1380G>T r.(?) p.(Met460Ile)
-?/. - c.1386T>C r.(?) p.(Ile462=)
+/. - c.1397_1403del r.(?) p.(Lys466Thrfs*2)
+/. - c.1397_1403del r.(?) p.(Lys466Thrfs*2)
+/. - c.1397_1403del r.(?) p.(Lys466Thrfs*2)
-/. - c.1442+11T>C r.(=) p.(=)
-/. - c.1442+11T>C r.(=) p.(=)
-/. - c.1442+11T>C r.(=) p.(=)
+/. - c.1443-2A>T r.spl p.?
?/. - c.1456_1458dup r.(?) p.(Leu486dup)
-?/. - c.1513A>T r.(?) p.(Ile505Leu)
-?/. - c.*158_*159insA r.(=) p.(=)
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