Transcript #00001544 (NM_001793.4, CDH3 gene)

Transcript name cadherin 3, type 1, P-cadherin (placental)
Gene name CDH3 (cadherin 3, type 1, P-cadherin (placental))
Chromosome 16
Transcript - NCBI ID NM_001793.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_001784.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 13:39:18 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.? r.(?) p.(Tyr249*)
+?/. - c.? r.(?) p.(Gly277Asp)
+/. - c.? r.(?) p.(Met327Ilefs*23)
+?/. - c.? r.(?) p.(Val734Met)
+?/. - c.3G>A r.(?) p.(Met1?)
-/. - c.141C>G r.(?) p.(Pro47=)
+?/. - c.160+1G>A r.spl p.(?)
+?/. - c.160+1G>A r.spl p.(?)
+?/. - c.160+1G>A r.spl p.(?)
+?/. - c.160+1G>A r.spl p.(?)
+?/. - c.160+1G>A r.spl p.(?)
+?/. - c.160+1G>A r.spl p.(?)
-?/. - c.214G>A r.(?) p.(Asp72Asn)
?/. - c.226C>T r.(?) p.(Arg76Trp)
+/. - c.307C>T r.(?) p.(Arg103*)
+?/. - c.316_317del r.(?) p.(Lys106Glufs*12)
+?/. - c.335C>T r.(?) p.(Ala112Val)
+?/. - c.335C>T r.(?) p.(Ala112Val)
-?/. - c.345T>C r.(?) p.(Ser115=)
-?/. - c.390+4C>G r.spl? p.?
?/. - c.390+5G>A r.spl? p.?
-?/. - c.410G>A r.(?) p.(Arg137Lys)
-/. - c.444G>A r.(?) p.(Pro148=)
-?/. - c.462T>G r.(?) p.(Pro154=)
?/. - c.505_507del r.(?) p.(Leu169del)
-?/. - c.507G>A r.(?) p.(Leu169=)
+/. - c.613G>A r.(?) p.(Val205Met)
-?/. - c.805A>C r.(?) p.(Met269Leu)
-?/. - c.805A>C r.(?) p.(Met269Leu)
-?/. - c.805A>C r.(?) p.(Met269Leu)
+/. - c.829del r.(?) p.(Gly277Alafs*20)
+/. - c.830del r.(?) p.(Gly277Alafs*20)
+/. - c.830del r.(?) p.(Gly277Alafs*20)
?/. - c.854G>T r.(?) p.(Gly285Val)
-?/. - c.867+3G>T r.spl? p.?
-/. - c.868-17C>T r.(=) p.(=)
?/. - c.909G>T r.(?) p.(Met303Ile)
-?/. - c.909G>T r.(?) p.(Met303Ile)
-/. - c.909G>T r.(?) p.(Met303Ile)
?/. - c.909G>T r.(?) p.(Met303Ile)
?/. - c.919G>A r.(?) p.(Gly307Ser)
+?/. - c.977C>A r.(?) p.(Pro326His)
-/. - c.996+13C>T r.(=) p.(=)
-?/. - c.1011G>C r.(?) p.(Val337=)
?/. - c.1033G>A r.(?) p.(Glu345Lys)
?/. - c.1037T>C r.(?) p.(Val346Ala)
+?/. - c.1063G>T r.(?) p.(Asp355Tyr)
+?/. - c.1063G>T r.(?) p.(Asp355Tyr)
+/. - c.1085G>A r.(?) p.(Trp362*)
+?/. - c.1086G>A r.(?) p.(Trp362*)
+/. 9 c.1086G>A r.(?) p.(Trp362Ter)
?/. - c.1111G>A r.(?) p.(Gly371Ser)
-?/. - c.1116C>T r.(?) p.(=)
-?/. - c.1117G>A r.(?) p.(Asp373Asn)
-?/. - c.1117G>A r.(?) p.(Asp373Asn)
?/. - c.1120G>A r.(?) p.(Gly374Arg)
+/. - c.1182+1G>A r.spl? p.?
-/. - c.1236C>T r.(?) p.(Asn412=)
-?/. - c.1257G>A r.(?) p.(=)
-?/. - c.1285G>A r.(?) p.(Val429Ile)
+?/. 10 c.1291_1294del r.(?) p.(Val431Argfs*3)
?/. - c.1298A>G r.(?) p.(Asp433Gly)
?/. - c.1308G>C r.(?) p.(Glu436Asp)
-/. - c.1339G>A r.(?) p.(Val447Ile)
?/. - c.1359C>G r.(?) p.(Ile453Met)
-?/. - c.1436T>C r.(?) p.(Leu479Pro)
?/. - c.1436T>C r.(?) p.(Leu479Pro)
?/. - c.1436T>C r.(?) p.(Leu479Pro)
-?/. - c.1436T>C r.(?) p.(Leu479Pro)
-?/. - c.1443C>T r.(?) p.(Asp481=)
-?/. - c.1443C>T r.(?) p.(Asp481=)
-?/. - c.1500C>T r.(?) p.(Thr500=)
+?/. - c.1508G>A r.(?) p.(Arg503His)
+/. 11 c.1508G>A r.(?) p.(Arg503His)
+?/. 11i_13i c.(1570+1_1571-1)_(2002+1_2003-1)del r.? p.?
?/. - c.1589G>T r.(?) p.(Gly530Val)
?/. - c.1592C>T r.(?) p.(Thr531Met)
?/. - c.1593G>A r.(?) p.(Thr531=)
?/. 12 c.1607T>C r.(?) p.(Leu536Pro)
?/. - c.1648C>T r.(?) p.(Pro550Ser)
-?/. - c.1654C>G r.(?) p.(Gln552Glu)
-?/. - c.1677C>T r.(?) p.(Ser559=)
-?/. - c.1681G>A r.(?) p.(Val561Met)
-?/. - c.1681G>A r.(?) p.(Val561Met)
?/. - c.1703C>T r.(?) p.(Thr568Met)
+/. - c.1795+1G>A r.spl? p.?
+?/. - c.1795+1G>A r.spl? p.?
+?/. - c.1795+1G>C r.spl? p.?
+?/. - c.1795+1G>C r.spl? p.?
+?/. - c.1796-2A>G r.spl? p.?
-?/. - c.1851G>A r.(?) p.(Val617=)
-?/. - c.1893G>A r.(?) p.(Thr631=)
-?/. - c.1933G>A r.(?) p.(Glu645Lys)
-?/. - c.1942C>T r.(?) p.(Pro648Ser)
-/. - c.1956G>A r.(?) p.(Lys652=)
+?/. - c.2002+5G>C r.spl? p.?
?/. - c.2041C>T r.(?) p.(Arg681Trp)
-/. - c.2058C>T r.(?) p.(Pro686=)
-?/. - c.2058C>T r.(?) p.(Pro686=)
?/. - c.2092G>A r.(?) p.(Val698Ile)
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