Transcript #00016802 (NM_005041.4, PRF1 gene)

Transcript name transcript variant 1
Gene name PRF1 (perforin 1 (pore forming protein))
Chromosome 10
Transcript - NCBI ID NM_005041.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_005032.2
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

95 entries on 1 page. Showing entries 1 - 95.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.10C>T r.(?) p.(Arg4Cys)
-?/. - c.11G>A r.(?) p.(Arg4His)
-?/. - c.11G>A r.(?) p.(Arg4His)
+/. - c.50del r.(?) p.(Leu17Argfs*34)
+/. - c.50del r.(?) p.(Leu17Argfs*34)
+/. - c.65del r.(?) p.(Pro22Argfs*29)
?/. - c.82C>T r.(?) p.(Arg28Cys)
-?/. - c.96G>A r.(?) p.(Lys32=)
-/. - c.96G>A r.(?) p.(Lys32=)
?/. - c.97C>T r.(?) p.(Arg33Cys)
-?/. - c.111C>T r.(?) p.(Phe37=)
?/. - c.260G>A r.(?) p.(Arg87His)
?/. - c.260G>A r.(?) p.(Arg87His)
?/. - c.272C>T r.(?) p.(Ala91Val)
-/. - c.272C>T r.(?) p.(Ala91Val)
?/. - c.272C>T r.(?) p.(Ala91Val)
-/. - c.272C>T r.(?) p.(Ala91Val)
?/. - c.355C>T r.(?) p.(Arg119Trp)
?/. - c.368G>A r.(?) p.(Arg123His)
-?/. - c.368G>A r.(?) p.(Arg123His)
-?/. - c.381C>T r.(?) p.(Asn127=)
+/. - c.394G>A r.(?) p.(Gly132Arg)
-/. - c.435G>A r.(=) p.(=)
-/. - c.444C>T r.(?) p.(Ala148=)
+/. - c.445G>A r.(?) p.(Gly149Ser)
+/. - c.445G>A r.(?) p.(Gly149Ser)
?/. - c.445G>A r.(?) p.(Gly149Ser)
+/. 2 c.445G>A r.(?) p.(Gly149Ser)
?/. - c.462A>G r.(=) p.(=)
-?/. - c.489C>T r.(?) p.(His163=)
-?/. - c.519G>A r.(?) p.(Thr173=)
-?/. - c.519G>A r.(?) p.(Thr173=)
-?/. - c.528C>T r.(?) p.(Cys176=)
-?/. - c.528C>T r.(?) p.(Cys176=)
-?/. - c.528C>T r.(?) p.(Cys176=)
-?/. - c.540-4G>A r.spl? p.?
-?/. - c.632C>T r.(?) p.(Ala211Val)
-?/. - c.640A>G r.(?) p.(Arg214Gly)
+/. - c.658G>A r.(?) p.(Gly220Ser)
?/. - c.666C>A r.(?) p.(His222Gln)
?/. - c.666C>A r.(?) p.(His222Gln)
+/. - c.673C>T r.(?) p.(Arg225Trp)
+?/. - c.673C>T r.(?) p.(Arg225Trp)
?/. - c.674G>A r.(?) p.(Arg225Gln)
-?/. - c.702G>A r.(?) p.(Ser234=)
-?/. - c.726C>T r.(?) p.(=)
?/. - c.755A>G r.(?) p.(Asn252Ser)
-/. - c.755A>G r.(?) p.(Asn252Ser)
-?/. - c.755A>G r.(?) p.(Asn252Ser)
-?/. - c.755A>G r.(?) p.(Asn252Ser)
+/. - c.808_812del r.(?) p.(Gly270Hisfs*9)
?/. - c.812_814del r.(?) p.(Ser271del)
-/. - c.822C>T r.(?) p.(Ala274=)
?/. - c.836G>A r.(?) p.(Cys279Tyr)
+/. - c.853_855del r.(?) p.(Lys285del)
+?/. - c.853_855del r.(?) p.(Lys285del)
+/. - c.853_855del r.(?) p.(Lys285del)
-?/. - c.890G>C r.(?) p.(Arg297Pro)
-/. - c.900C>T r.(?) p.(His300=)
-/. - c.900C>T r.(?) p.(His300=)
-/. - c.900C>T r.(?) p.(His300=)
-?/. - c.903G>A r.(?) p.(Ser301=)
-?/. - c.945G>A r.(?) p.(Leu315=)
?/. - c.961G>A r.(?) p.(Gly321Arg)
-?/. - c.963G>T r.(?) p.(Gly321=)
-?/. - c.966C>T r.(?) p.(Pro322=)
?/. - c.1001G>A r.(?) p.(Gly334Asp)
+?/. - c.1018G>A r.(?) p.(Asp340Asn)
+/. 3 c.1081A>T r.(?) p.(Arg361Trp)
?/. - c.1111A>G r.(?) p.(Arg371Gly)
+/. - c.1122G>A r.(?) p.(Trp374Ter)
+/. - c.1122G>A r.(?) p.(Trp374Ter)
?/. - c.1144C>T r.(?) p.(Pro382Ser)
?/. - c.1144C>T r.(?) p.(Pro382Ser)
?/. - c.1153C>T r.(?) p.(Arg385Trp)
-?/. - c.1212C>T r.(?) p.(Thr404=)
?/. - c.1229G>C r.(?) p.(Arg410Pro)
-?/. - c.1254G>A r.(?) p.(Glu418=)
+?/. - c.1298C>T r.(?) p.(Thr433Ile)
-?/. - c.1305G>A r.(?) p.(Thr435=)
?/. - c.1310C>T r.(?) p.(Ala437Val)
?/. - c.1310C>T r.(?) p.(Ala437Val)
?/. - c.1310C>T r.(?) p.(Ala437Val)
+?/. - c.1349C>T r.(?) p.(Thr450Met)
+/. - c.1349C>T r.(?) p.(Thr450Met)
?/. - c.1357G>A r.(?) p.(Val453Met)
?/. - c.1373A>C r.(?) p.(Asn458Thr)
?/. - c.1444G>T r.(?) p.(Val482Phe)
-?/. - c.1470C>T r.(?) p.(Asp490=)
?/. - c.1471G>A r.(?) p.(Asp491Asn)
?/. - c.1501C>T r.(?) p.(Pro501Ser)
?/. - c.1562A>G r.(?) p.(Tyr521Cys)
-?/. - c.1620A>G r.(?) p.(Gln540=)
-/. - c.1620A>G r.(?) p.(Gln540=)
-/. - c.*174T>C r.(=) p.(=)
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