Transcript #00024280 (NM_024110.4, CARD14 gene)

Transcript name transcript variant 1
Gene name CARD14 (caspase recruitment domain family, member 14)
Chromosome 17
Transcript - NCBI ID NM_024110.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_077015.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2017-06-29 15:52:52 +02:00 (CEST)
Date last edited N/A


Variants

281 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-20-19C>T r.(=) p.(=)
?/. - c.34dup r.(?) p.(Thr12Asnfs*87)
-?/. - c.35C>T r.(?) p.(Thr12Met)
+/. ? c.112C>T r.(?) p.(Arg38Cys)
?/. - c.122C>T r.(?) p.(Pro41Leu)
-?/. - c.159C>T r.(?) p.(Asp53=)
+/. ? c.185G>A r.(?) p.(Arg62Gln)
-/. - c.185G>A r.(?) p.(Arg62Gln)
-?/. - c.205C>A r.(?) p.(Arg69=)
?/. - c.205C>T r.(?) p.(Arg69Trp)
?/. - c.211G>A r.(?) p.(Gly71Arg)
-?/. - c.211+7G>A r.(=) p.(=)
?/. - c.234G>T r.(?) p.(Lys78Asn)
-?/. - c.345T>C r.(?) p.(Phe115=)
-?/. - c.345T>C r.(?) p.(Phe115=)
+/. ? c.349G>A r.(?) p.(Gly117Ser)
+/. - c.349+1G>A r.spl? p.?
+/. - c.356T>C r.(?) p.(Met119Thr)
-?/. - c.378G>A r.(?) p.(Glu126=)
-?/. - c.378G>A r.(?) p.(Glu126=)
?/. - c.407A>C r.(?) p.(Gln136Pro)
+/. ? c.413A>C r.(?) p.(Glu138Ala)
+/. ? c.424G>A r.(?) p.(Glu142Lys)
+/. ? c.425A>G r.(?) p.(Glu142Gly)
+?/. - c.440_442del r.(?) p.(Glu147del)
+/. ? c.449T>G r.(?) p.(Leu150Arg)
-?/. - c.449T>G r.(?) p.(Leu150Arg)
-?/. - c.449T>G r.(?) p.(Leu150Arg)
-?/. - c.480G>A r.(?) p.(Leu160=)
?/. - c.496C>T r.(?) p.(Arg166Cys)
+/. ? c.511C>A r.(?) p.(His171Asn)
+/. ? c.536G>A r.(?) p.(Arg179His)
?/. - c.549G>C r.(?) p.(Glu183Asp)
-?/. - c.570G>A r.(?) p.(Glu190=)
+/. ? c.571G>T r.(?) p.(Val191Leu)
+/. ? c.599G>A r.(?) p.(Ser200Asn)
-?/. - c.599G>A r.(?) p.(Ser200Asn)
-?/. - c.599G>T r.(?) p.(Ser200Ile)
-?/. - c.676-30C>T r.(=) p.(=)
-?/. - c.676-7C>T r.(=) p.(=)
-/. - c.676-6G>A r.(=) p.(=)
+?/. - c.681T>G r.(?) p.(Tyr227Ter)
-?/. - c.709A>C r.(?) p.(Asn237His)
-?/. - c.824G>A r.(?) p.(Arg275His)
-?/. - c.843+16C>T r.(=) p.(=)
+/. ? c.854A>G r.(?) p.(Asp285Gly)
?/. - c.881C>T r.(?) p.(Ala294Val)
?/. - c.881C>T r.(?) p.(Ala294Val)
?/. - c.892C>T r.(?) p.(Arg298*)
-?/. - c.922C>T r.(?) p.(Leu308=)
?/. - c.925C>T r.(?) p.(Arg309Trp)
-?/. - c.960G>A r.(?) p.(Glu320=)
+?/. - c.964-1G>A r.spl? p.?
-?/. - c.1012A>G r.(?) p.(Met338Val)
-?/. - c.1065C>T r.(?) p.(Cys355=)
-?/. - c.1065C>T r.(?) p.(Cys355=)
-/. - c.1090-34G>A r.(=) p.(=)
-?/. - c.1090-27C>T r.(=) p.(=)
?/. - c.1091C>T r.(?) p.(Ala364Val)
-?/. - c.1134C>G r.(?) p.(Ser378Arg)
-?/. - c.1182C>T r.(?) p.(Asp394=)
?/. - c.1198C>T r.(?) p.(Arg400Cys)
-?/. - c.1199G>A r.(?) p.(Arg400His)
-/. - c.1264G>A r.(?) p.(Glu422Lys)
-/. - c.1264G>A r.(?) p.(Glu422Lys)
-?/. - c.1277G>A r.(?) p.(Arg426Gln)
-?/. - c.1326C>G r.(?) p.(Asp442Glu)
-?/. - c.1342G>A r.(?) p.(Val448Ile)
-?/. - c.1356+4C>T r.spl? p.?
-?/. - c.1356+5G>A r.spl? p.?
-?/. - c.1356+18G>A r.(=) p.(=)
-?/. - c.1356+18_1356+19del r.(=) p.(=)
+?/. - c.1357-1G>A r.spl? p.?
-?/. - c.1385C>T r.(?) p.(Thr462Met)
-?/. - c.1415G>A r.(?) p.(Arg472His)
-?/. - c.1463T>C r.(?) p.(Val488Ala)
-/. - c.1499+13G>A r.(=) p.(=)
?/. - c.1499+27_1499+55del r.(=) p.(=)
-?/. - c.1499+27_1499+55del r.(=) p.(=)
-/. - c.1517C>T r.(?) p.(Pro506Leu)
-/. - c.1517C>T r.(?) p.(Pro506Leu)
?/. - c.1534G>T r.(?) p.(Ala512Ser)
-?/. - c.1557C>T r.(?) p.(Gly519=)
-?/. - c.1590G>A r.(?) p.(Thr530=)
-?/. - c.1594+4A>G r.spl? p.?
-?/. - c.1601C>T r.(?) p.(Pro534Leu)
-/. - c.1641G>C r.(?) p.(Arg547Ser)
-?/. - c.1658+3A>G r.spl? p.?
-/. - c.1662C>T r.(?) p.(Gly554=)
-/. - c.1662C>T r.(?) p.(Gly554=)
?/. - c.1703A>C r.(?) p.(Gln568Pro)
?/. - c.1703A>C r.(?) p.(Gln568Pro)
-?/. - c.1738C>T r.(?) p.(Leu580=)
-?/. - c.1772C>T r.(?) p.(Thr591Met)
+/. ? c.1778T>A r.(?) p.(Ile593Asn)
-/. - c.1789C>T r.(?) p.(Arg597Trp)
-/. - c.1789C>T r.(?) p.(Arg597Trp)
?/. - c.1805C>T r.(?) p.(Ser602Leu)
-?/. - c.1806G>A r.(?) p.(Ser602=)
./. - c.1808C>T r.(?) p.(Ala603Val)
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