Transcript #00007401 (NM_020223.3, FAM20C gene)

Transcript name family with sequence similarity 20, member C
Gene name FAM20C (family with sequence similarity 20, member C)
Chromosome 7
Transcript - NCBI ID NM_020223.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_064608.2
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

99 entries on 1 page. Showing entries 1 - 99.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. _1_10_ c.(-156720_-148270)_(863+21018_*223785)del r.0 p.0
+/. _1_3_ c.(?_-181)_(863+1_?)del r.0? p.0?
+/. - c.0 r.0 p.0
+/. _1_10_ c.0 r.0 p.0
-?/. - c.6G>A r.(?) p.(=)
-?/. - c.23G>A r.(?) p.(Arg8Gln)
-?/. - c.46G>T r.(?) p.(Val16Leu)
-?/. - c.46G>T r.(?) p.(Val16Leu)
-?/. - c.55G>T r.(?) p.(Val19Leu)
-?/. - c.66G>A r.(?) p.(=)
+/. - c.117A>T r.(?) p.(=)
-?/. - c.200C>A r.(?) p.(Pro67His)
?/. - c.202G>T r.(?) p.(Gly68Trp)
+?/. 1 c.307_308dup r.(?) p.(Ser104ArgfsTer27)
+/. - c.456del r.(?) p.(Gly153Alafs*34)
+?/. - c.456dup r.(456dup) p.(Gly153Argfs*56)
+/. - c.456dup r.(?) p.(Gly153Argfs*56)
+/. - c.474del r.(?) p.(Ser159Profs*28)
+/. - c.496G>T r.(?) p.(Glu166*)
?/. - c.565G>T r.(?) p.(Asp189Tyr)
-?/. - c.646G>A r.(?) p.(Gly216Arg)
-/. - c.646G>A r.(?) p.(Gly216Arg)
+/. - c.676T>A r.(?) p.(Trp226Arg)
-?/. - c.733G>A r.(?) p.(Ala245Thr)
+/. - c.773T>A r.(?) p.(Ile258Asn)
+/. 2i c.784+5G>C r.606_784del p.Trp202CysfsTer37
+/. - c.796C>T r.(?) p.(Arg266Cys)
+/. - c.803C>T r.(?) p.(Thr268Met)
+/. - c.838G>A r.(?) p.(Gly280Arg)
+/. - c.863+5G>C r.spl p.?
?/. - c.895T>A r.(?) p.(Phe299Ile)
+/. - c.905del r.(?) p.(Phe302Serfs*35)
+/. - c.906C>A r.(?) p.(Phe302Leu)
+/. - c.915C>A r.(?) p.(Tyr305*)
+?/. 4_4i c.952_956+30dup r.(?) p.(?,=)
-?/. - c.953_956+30dup r.spl? p.?
-?/. - c.953_956+30dup r.spl? p.?
-/. - c.953_956+30dup r.spl? p.?
-?/. - c.953_956+30dup r.spl? p.?
+?/. - c.956G>A r.(?) p.(Arg319Lys)
+?/. - c.956+5G>C r.spl p.?
+?/. - c.957-3C>G r.spl p.?
+/. - c.982C>T r.(?) p.(Pro328Ser)
-?/. - c.999G>A r.(?) p.(Met333Ile)
+/. - c.1007T>G r.(?) p.(Met336Arg)
?/. - c.1018A>G r.(?) p.(Ile340Val)
?/. - c.1021C>T r.(?) p.(Arg341Trp)
+/. - c.1071A>G r.spl p.?
+/. - c.1094G>A r.(?) p.(Gly365Asp)
+/. - c.1108_1112dup r.(?) p.(Ser372Thrfs*60)
?/. - c.1118C>T r.(?) p.(Thr373Met)
+/. - c.1135G>A r.(?) p.(Gly379Arg)
+/. - c.1135G>A r.(?) p.(Gly379Arg)
+/. - c.1136G>A r.(?) p.(Gly379Glu)
+/. - c.1163T>G r.(?) p.(Leu388Arg)
?/. - c.1182C>G r.(?) p.(Asp394Glu)
+/. - c.1219T>G r.(?) p.(Trp407Gly)
+/. - c.1222C>T r.(?) p.(Arg408Trp)
+/. - c.1225C>T r.(?) p.(Arg409Cys)
+/. - c.1225C>T r.(?) p.(Arg409Cys)
-/. - c.1228T>A r.(?) p.(Ser410Thr)
-?/. - c.1228T>A r.(?) p.(Ser410Thr)
?/. - c.1228T>A r.(?) p.(Ser410Thr)
+/. - c.1228T>A r.(?) p.(Ser410Thr)
?/. - c.1241G>A r.(?) p.(Arg414His)
+/. - c.1255T>C r.(?) p.(Trp419Arg)
+/. - c.1351G>A r.(?) p.(Asp451Asn)
+/. - c.1351G>A r.(?) p.(Asp451Asn)
+/. - c.1351G>A r.(?) p.(Asp451Asn)
?/. - c.1363+5G>A r.spl? p.?
+/. - c.1364-2A>G r.spl p.?
+/. - c.1375C>G r.(?) p.(Arg459Gly)
?/. - c.1376G>A r.(?) p.(Arg459His)
+/. - c.1446-1G>A r.spl p.?
+/. - c.1487C>T r.(?) p.(Pro496Leu)
+?/. - c.1528C>T r.(?) p.(Arg510Cys)
?/. - c.1529G>A r.(?) p.(Arg510His)
+/. - c.1557C>G r.(?) p.(Tyr519*)
-?/. - c.1559A>G r.(?) p.(Lys520Arg)
?/. - c.1643G>A r.(?) p.(Arg548Gln)
+/. - c.1645C>T r.(?) p.(Arg549Trp)
+/. - c.1645C>T r.(?) p.(Arg549Trp)
-?/. - c.1652G>A r.(?) p.(Arg551His)
?/. - c.1654G>A r.(?) p.(Val552Ile)
-/. - c.1659G>T r.(?) p.(Val553=)
-/. - c.1672C>T r.(?) p.(Arg558Trp)
?/. - c.1672C>T r.(?) p.(Arg558Trp)
-?/. - c.1672C>T r.(?) p.(Arg558Trp)
+/. - c.1672C>T r.(?) p.(Arg558Trp)
+/. - c.1672C>T r.(?) p.(Arg558Trp)
+/. 10 c.1680C>A r.(?) p.(Cys560*)
+/. - c.1680C>A r.(?) p.(Cys560*)
-?/. - c.1681G>A r.(?) p.(Val561Met)
?/. - c.1690A>C r.(?) p.(Asn564His)
-/. - c.1690A>G r.(?) p.(Asn564Asp)
?/. - c.1690A>G r.(?) p.(Asn564Asp)
?/. - c.1705G>A r.(?) p.(Val569Met)
?/. - c.1717G>A r.(?) p.(Asp573Asn)
-?/. - c.1741G>A r.(?) p.(Ala581Thr)
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