Transcript #00000348 (NM_002621.2, CFP gene)

Transcript name transcript variant 1
Gene name CFP (complement factor properdin)
Chromosome X
Transcript - NCBI ID NM_002621.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_002612.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 12:09:14 +02:00 (CEST)
Date last edited N/A


Variants

83 entries on 1 page. Showing entries 1 - 83.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. 2 c.13G>A r.(?) p.(Gly5Arg)
-?/. - c.76+12dup r.(=) p.(=)
-?/. - c.88G>A r.(?) p.(Val30Met)
-?/. - c.121G>A r.(?) p.(Gly41Ser)
-?/. - c.157G>A r.(?) p.(Val53Met)
-?/. - c.157G>A r.(?) p.(Val53Met)
-?/. - c.157G>A r.(?) p.(Val53Met)
?/. - c.209G>A r.(?) p.(Gly70Glu)
-?/. - c.227+18G>C r.(=) p.(=)
?/. - c.228-237dup r.(=) p.(=)
?/. - c.228-237dup r.(=) p.(=)
?/. - c.228-237dup r.(=) p.(=)
?/. - c.228-237dup r.(=) p.(=)
-/. - c.228-237dup r.(=) p.(=)
-/. - c.236G>A r.(?) p.(Arg79Gln)
?/. 4 c.359T>C r.(?) p.(Leu120Pro)
?/. - c.391C>G r.(?) p.(Gln131Glu)
-/. - c.391C>G r.(?) p.(Gln131Glu)
-?/. - c.403+9G>A r.(=) p.(=)
?/. - c.435G>T r.(?) p.(Trp145Cys)
-?/. - c.444C>T r.(?) p.(Cys148=)
-?/. - c.476G>A r.(?) p.(Arg159His)
?/. - c.575-8C>G r.(=) p.(=)
?/. - c.580G>A r.(?) p.(Gly194Arg)
?/. - c.580G>A r.(?) p.(Gly194Arg)
?/. - c.580G>A r.(?) p.(Gly194Arg)
-?/. - c.608C>G r.(?) p.(Thr203Ser)
-?/. - c.611C>T r.(?) p.(Pro204Leu)
-?/. - c.611C>T r.(?) p.(Pro204Leu)
?/. - c.631G>A r.(?) p.(Gly211Ser)
-?/. - c.663C>T r.(?) p.(Ser221=)
-?/. - c.663C>T r.(?) p.(Ser221=)
-?/. - c.663C>T r.(?) p.(Ser221=)
./. - c.665G>A r.(?) p.(Arg222His)
?/. - c.665G>A r.(?) p.(Arg222His)
?/. - c.680C>T r.(?) p.(Pro227Leu)
-/. - c.686C>G r.(?) p.(Pro229Arg)
-?/. - c.729C>T r.(?) p.(Tyr243=)
-?/. - c.747C>T r.(?) p.(Thr249=)
?/. - c.748G>A r.(?) p.(Gly250Ser)
?/. - c.748G>A r.(?) p.(Gly250Ser)
-?/. - c.748G>A r.(?) p.(Gly250Ser)
?/. - c.766+54G>T r.(=) p.(=)
?/. - c.766+54G>T r.(=) p.(=)
+/. - c.786_793del r.(?) p.(Trp263Cysfs*91)
?/. - c.865C>T r.(?) p.(Pro289Ser)
-?/. - c.894C>T r.(?) p.(Gly298=)
-?/. - c.895G>A r.(?) p.(Asp299Asn)
-?/. - c.895G>A r.(?) p.(Asp299Asn)
-?/. - c.895G>A r.(?) p.(Asp299Asn)
-?/. - c.913A>G r.(?) p.(Ile305Val)
-?/. - c.940+7A>G r.(=) p.(=)
-?/. - c.941-10G>A r.(=) p.(=)
-?/. - c.955G>A r.(?) p.(Asp319Asn)
+?/. - c.961T>G r.(?) p.(Trp321Gly)
+/. 8 c.962G>A r.(?) p.(Trp321Ter)
-?/. - c.1133-6T>C r.(=) p.(=)
?/. - c.1180C>T r.(?) p.(Pro394Ser)
?/. - c.1180C>T r.(?) p.(Pro394Ser)
?/. 9 c.1187G>A r.(?) p.(Gly396Glu)
-?/. - c.1224A>T r.(?) p.(Thr408=)
?/. - c.1239G>C r.(?) p.(Lys413Asn)
?/. - c.1245-100dup r.(=) p.(=)
?/. - c.1245-100_1245-99del r.(=) p.(=)
?/. - c.1245-99del r.(=) p.(=)
-?/. 9i c.1245-86T>C r.(?) p.(=)
-?/. 9i c.1245-86T>C r.(?) p.(=)
?/. 10 c.1284C>T r.(?) p.(=)
-?/. 10 c.1284C>T r.(?) p.(Asn428=)
-?/. 10 c.1284C>T r.(?) p.(Asn428=)
-/. - c.1284C>T r.(?) p.(Asn428=)
-/. - c.1284C>T r.(?) p.(Asn428=)
?/. - c.1328A>G r.(?) p.(Gln443Arg)
-?/. - c.*4466T>C r.(=) p.(=)
-?/. - c.*4519C>G r.(=) p.(=)
?/. - c.*4635C>G r.(=) p.(=)
-?/. - c.*4685G>A r.(=) p.(=)
-?/. - c.*4698C>G r.(=) p.(=)
-?/. - c.*4735G>T r.(=) p.(=)
-?/. - c.*4735G>T r.(=) p.(=)
?/. - c.*4898G>A r.(=) p.(=)
-?/. - c.*4910C>T r.(=) p.(=)
-?/. - c.*4910C>T r.(=) p.(=)
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