Transcript #00005445 (NM_004086.2, COCH gene)

Transcript name transcript variant 2
Gene name COCH (coagulation factor C homolog, cochlin (Limulus polyphemus))
Chromosome 14
Transcript - NCBI ID NM_004086.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_004077.1
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

84 entries on 1 page. Showing entries 1 - 84.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.7G>C r.(?) p.(Ala3Pro)
+/. 4 c.113G>A r.(?) p.(Gly38Asp)
-?/. - c.126G>C r.(?) p.(Arg42Ser)
-?/. - c.141T>C r.(?) p.(Asp47=)
-?/-? 4 c.141T>C r.(=) p.(=)
+/. - c.151C>T r.(?) p.(Pro51Ser)
+/. - c.151C>T r.(?) p.(Pro51Ser)
+/. - c.151C>T r.(?) p.(Pro51Ser)
+/+ 4 c.151C>T r.(?) p.(Pro51Ser)
+/. - c.151C>T r.(?) p.(Pro51Ser)
?/. - c.163C>G r.(?) p.(Pro55Ala)
+/+ 4 c.197T>G r.(?) p.(Val66Gly)
+?/. - c.202G>C r.(?) p.(Ala68Pro)
?/. - c.226G>A r.(?) p.(Ala76Thr)
-?/-? 4i c.239+7C>G r.(=) p.(=)
-?/. - c.257C>T r.(?) p.(Ser86Leu)
+/. - c.259G>T r.(?) p.(Gly87Trp)
+/+ 5 c.259G>T r.(?) p.(Gly87Trp)
+?/. - c.259G>T r.(?) p.(Gly87Trp)
+/+ 5 c.260G>T r.(?) p.(Gly87Val)
+/+ 5 c.263G>A r.(?) p.(Gly88Glu)
+/. - c.263G>A r.(?) p.(Gly88Glu)
?/? 5 c.263G>T r.(?) p.(Gly88Val)
+/+ 5 c.266C>A r.(?) p.(Pro89His)
-?/. - c.266C>A r.(?) p.(Pro89His)
-?/. - c.288T>C r.(?) p.(Pro96=)
+/. - c.292C>T r.292c>u|<0.1 p.(Arg98*)
+/+ 5 c.311_313del r.(?) p.(Val104del)
+/+ 5 c.326T>A r.(?) p.(Ile109Asn)
+?/. - c.326T>C r.(?) p.(Ile109Thr)
+/. 5 c.326T>C r.(?) p.(Ile109Thr)
+/+ 5 c.326T>C r.(?) p.(Ile109Thr)
+/. 5 c.341T>C r.(?) p.(Leu114Pro)
+/+ 5 c.349T>C r.(?) p.(Trp117Arg)
+/+ 5 c.355G>A r.(?) p.(Ala119Thr)
+?/. - c.361T>C r.(?) p.(Phe121Leu)
+/+ 5 c.362T>C r.(?) p.(Phe121Ser)
+/. - c.368T>A r.(?) p.(Val123Glu)
+/. 5 c.368T>A r.(?) p.(Val123Glu)
+/+ 8 c.485G>A r.(?) p.(Cys162Tyr)
-?/. - c.519C>T r.(?) p.(Ser173=)
+?/. - c.535C>T r.(?) p.(Arg179Cys)
-?/. - c.539G>A r.(?) p.(Arg180Gln)
-?/. - c.555G>A r.(?) p.(Lys185=)
-?/. - c.615C>T r.(?) p.(Gly205=)
-?/. - c.629+5C>T r.spl? p.?
-?/. - c.665_666del r.(?) p.(Phe222TyrfsTer19)
-?/. - c.734-17T>C r.(=) p.(=)
?/. - c.740C>G r.(?) p.(Ala247Gly)
-?/. - c.909G>A r.(?) p.(Lys303=)
?/. - c.971G>A r.(?) p.(Arg324Gln)
+/. - c.984_985dup r.984_985dup p.Phe329Serfs*16
?/. - c.1016C>T r.(?) p.(Thr339Ile)
-?/. - c.1047G>A r.(?) p.(Lys349=)
-/. - c.1055C>G r.(?) p.(Thr352Ser)
-/. - c.1055C>G r.(?) p.(Thr352Ser)
-/. - c.1055C>G r.(?) p.(Thr352Ser)
+?/. - c.1115T>C r.(?) p.(Ile372Thr)
+/+ 11 c.1115T>C r.(?) p.(Ile372Thr)
?/. - c.1150C>T r.(?) p.(Arg384Cys)
+/. 11 c.1159C>T r.(?) p.(Leu387Phe)
+/+ 11 c.1196_1213del r.(?) p.(Ile399_Ala404del)
?/. - c.1229A>G r.(?) p.(Gln410Arg)
?/. - c.1270T>G r.(?) p.(Tyr424Asp)
+?/+? 11 c.1303A>G r.(?) p.(Arg435Gly)
+?/. 11 c.1312C>T r.(?) p.(Arg438Cys)
?/. - c.1324G>C r.(?) p.(Gly442Arg)
-?/. - c.1348A>G r.(?) p.(Ile450Val)
-?/. - c.1348A>G r.(?) p.(Ile450Val)
?/. - c.1436A>G r.(?) p.(Tyr479Cys)
+/+ 11 c.1459G>C r.(?) p.(Ala487Pro)
-/. - c.1477+9C>A r.(=) p.(=)
-/. - c.1477+9C>A r.(=) p.(=)
?/. - c.1478-15A>G r.(=) p.(=)
?/. - c.1487T>A r.(?) p.(Ile496Asn)
+?/+? 12 c.1529A>G r.(?) p.(Lys510Arg)
+/+ 12 c.1535T>C r.(?) p.(Met512Thr)
+/+ 12 c.1580T>G r.(?) p.(Phe527Cys)
-?/. - c.1591G>C r.(?) p.(Glu531Gln)
?/. - c.1591G>C r.(?) p.(Glu531Gln)
+/+ 12 c.1624T>C r.(?) p.(Cys542Arg)
+/+ 12 c.1625G>A r.(?) p.(Cys542Tyr)
+/+ 12 c.1625G>T r.(?) p.(Cys542Phe)
-/. - c.*27A>T r.(=) p.(=)
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