Transcript #00003753 (NM_001735.2, C5 gene)

Transcript name complement component 5
Gene name C5 (complement component 5)
Chromosome 9
Transcript - NCBI ID NM_001735.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001726.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

88 entries on 1 page. Showing entries 1 - 88.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-24522C>T r.(?) p.(=)
?/. - c.-24508G>A r.(?) p.(=)
-?/. - c.-24498C>T r.(?) p.(=)
?/. - c.95G>A r.(?) p.(Arg32His)
-?/. - c.192T>C r.(?) p.(Phe64=)
-?/. - c.259-3C>A r.spl? p.?
?/. - c.267A>C r.(?) p.(=)
?/. - c.352C>T r.(?) p.(Pro118Ser)
-?/. - c.433G>A r.(?) p.(Val145Ile)
-?/. - c.460C>T r.(?) p.(Pro154Ser)
?/. - c.471A>T r.(?) p.(Arg157Ser)
?/. - c.471A>T r.(?) p.(Arg157Ser)
?/. - c.551C>A r.(?) p.(Ser184Tyr)
-?/. - c.691A>G r.(?) p.(Ile231Val)
-?/. - c.758+20dup r.(=) p.(=)
?/. - c.877A>G r.(?) p.(Ile293Val)
-?/. - c.989T>C r.(?) p.(Ile330Thr)
-?/. - c.989T>C r.(?) p.(Ile330Thr)
-?/. - c.989T>C r.(?) p.(Ile330Thr)
-/. - c.1000+27_1000+34dup r.(=) p.(=)
-?/. - c.1060C>A r.(?) p.(Leu354Met)
?/. - c.1060C>A r.(?) p.(Leu354Met)
?/. - c.1147G>T r.(?) p.(Val383Leu)
-/. - c.1155A>G r.(?) p.(Gly385=)
?/. - c.1286C>T r.(?) p.(Thr429Met)
?/. - c.1418A>G r.(?) p.(His473Arg)
-?/. - c.1424C>T r.(?) p.(Ala475Val)
-/. - c.1461C>T r.(?) p.(Thr487=)
-/. - c.1632C>T r.(?) p.(Tyr544=)
-/. - c.1632C>T r.(?) p.(Tyr544=)
?/. - c.1636G>T r.(?) p.(Val546Phe)
?/. - c.1901G>T r.(?) p.(Cys634Phe)
-?/. - c.1929C>G r.(?) p.(=)
-?/. - c.1989A>G r.(?) p.(Gln663=)
?/. - c.2059+3A>G r.spl? p.?
-?/. - c.2059+16T>A r.(=) p.(=)
-?/. - c.2163G>A r.(?) p.(=)
-?/. - c.2163G>A r.(?) p.(=)
-?/. - c.2177A>G r.(?) p.(Lys726Arg)
-?/. - c.2257+19A>C r.(=) p.(=)
-?/. - c.2362T>G r.(?) p.(Phe788Val)
-?/. - c.2362T>G r.(?) p.(Phe788Val)
-/. - c.2404G>A r.(?) p.(Val802Ile)
-/. - c.2404G>A r.(?) p.(Val802Ile)
-?/. - c.2420C>T r.(?) p.(Thr807Ile)
-?/. - c.2420C>T r.(?) p.(Thr807Ile)
?/. - c.2598del r.(?) p.(Cys866*)
+/. - c.2654G>A r.(?) p.(Arg885His)
-?/. - c.2941+10C>G r.(=) p.(=)
-?/. - c.3029C>T r.(?) p.(Ala1010Val)
-?/. - c.3029C>T r.(?) p.(Ala1010Val)
-?/. - c.3029C>T r.(?) p.(Ala1010Val)
-?/. - c.3029C>T r.(?) p.(Ala1010Val)
-?/. - c.3068A>G r.(?) p.(His1023Arg)
?/. - c.3118A>G r.(?) p.(Ile1040Val)
-?/. - c.3154+13del r.(=) p.(=)
-?/. - c.3199A>C r.(?) p.(Ser1067Arg)
?/. - c.3199A>C r.(?) p.(Ser1067Arg)
-?/. - c.3391-10T>C r.(=) p.(=)
-?/. - c.3463G>A r.(?) p.(Ala1155Thr)
-?/. - c.3659-6G>A r.(=) p.(=)
-?/. - c.3732G>A r.(?) p.(Thr1244=)
-?/. - c.3871A>G r.(?) p.(Ile1291Val)
-?/. - c.3871A>G r.(?) p.(Ile1291Val)
?/. - c.3926T>C r.(?) p.(Leu1309Ser)
-/. - c.4017+17C>G r.(=) p.(=)
./. - c.4017+17C>G r.(=) p.(=)
-/. - c.4018-21_4018-18del r.(=) p.(=)
?/. - c.4030G>A r.(?) p.(Asp1344Asn)
?/. - c.4081-6A>G r.(=) p.(=)
-?/. - c.4162+10G>A r.(=) p.(=)
-/. - c.4163-12C>T r.(=) p.(=)
-?/. - c.4166C>T r.(?) p.(Ser1389Phe)
?/. - c.4204A>G r.(?) p.(Ile1402Val)
-/. - c.4221-13T>C r.(=) p.(=)
-/. - c.4266G>A r.(?) p.(=)
-/. - c.4311A>C r.(?) p.(Glu1437Asp)
-?/. - c.4321G>T r.(?) p.(Ala1441Ser)
-?/. - c.4323+9T>A r.(=) p.(=)
-?/. - c.4488C>T r.(?) p.(Tyr1496=)
?/. - c.4572G>A r.(?) p.(=)
-?/. - c.4588+6C>T r.(=) p.(=)
-?/. - c.4785C>T r.(?) p.(Asp1595=)
-/. - c.4806A>G r.(?) p.(Lys1602=)
-?/. - c.4968G>C r.(?) p.(Ser1656=)
+/. - c.4972C>T r.(?) p.(Gln1658*)
?/. - c.4994A>G r.(?) p.(Asp1665Gly)
-?/. - c.5011A>G r.(?) p.(Ile1671Val)
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