Transcript #00023955 (NM_000195.3, HPS1 gene)

Transcript name transcript variant 1
Gene name HPS1 (Hermansky-Pudlak syndrome 1)
Chromosome 10
Transcript - NCBI ID NM_000195.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000186.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2014-07-24 22:34:28 +02:00 (CEST)
Date last edited N/A


Variants

120 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. 1i_2i c.(-106+1_-105-1)_(1+1_1-1)del r.? p.?
+/. 3 c.2T>A r.(?) p.(Met1?)
-/. - c.11T>C r.(?) p.(Val4Ala)
+?/. - c.16dup r.(?) p.(Val6Glyfs*4)
?/. - c.16G>A r.(?) p.(Val6Met)
-/. - c.27G>C r.(?) p.(Glu9Asp)
-/. - c.27G>C r.(?) p.(Glu9Asp)
+/. 3 c.34dup r.(?) p.(Glu12GlyfsTer12)
-?/. - c.59A>G r.(?) p.(Gln20Arg)
-/. - c.90C>T r.(?) p.(Phe30=)
+/. - c.212_215del r.(?) p.(Cys71SerfsTer52)
+/. 13 c.217del r.(?) p.(Ser73ProfsTer51)
?/. - c.222G>A r.(?) p.(Thr74=)
-?/. - c.255+9A>G r.(=) p.(=)
?/. - c.260G>T r.(?) p.(Gly87Val)
-?/. - c.266G>A r.(?) p.(Cys89Tyr)
?/. - c.284A>G r.(?) p.(Asn95Ser)
-/. - c.297C>T r.(?) p.(Thr99=)
?/. - c.353T>G r.(?) p.(Val118Gly)
+/. - c.391C>T r.(?) p.(Arg131Ter)
?/. - c.399-5C>A r.spl? p.?
+/. - c.437G>A r.(?) p.(Trp146*)
+/. - c.437G>A r.(?) p.(Trp146*)
-?/. - c.478C>T r.(?) p.(Arg160Trp)
+/. 6i c.507+1G>A r.spl p.?
-?/. - c.507+13C>T r.(=) p.(=)
+/. - c.517C>T r.(?) p.(Arg173*)
-/. - c.557C>T r.(?) p.(Ala186Val)
-/. - c.558G>A r.(?) p.(Ala186=)
-?/. - c.571G>A r.(?) p.(Val191Ile)
-/. - c.597C>T r.(?) p.(Pro199=)
?/. - c.681C>G r.(?) p.(Ser227Arg)
?/. - c.695C>T r.(?) p.(Ala232Val)
+/. 8 c.716T>C r.(?) p.(Leu239Pro)
+/. 8 c.716T>C r.(?) p.(Leu239Pro)
+/. 8 c.716T>C r.(?) p.(Leu239Pro)
?/. - c.737C>T r.(?) p.(Pro246Leu)
?/. - c.737C>T r.(?) p.(Pro246Leu)
-/. - c.759C>T r.(?) p.(Asp253=)
-?/. - c.778C>T r.(?) p.(Arg260Trp)
-?/. - c.778C>T r.(?) p.(Arg260Trp)
-/. - c.779G>A r.(?) p.(Arg260Gln)
-/. - c.779G>A r.(?) p.(Arg260Gln)
-?/. - c.779G>A r.(?) p.(Arg260Gln)
?/. - c.787C>T r.(?) p.(Arg263Trp)
+/. - c.807del r.(?) p.(Val270CysfsTer61)
?/. - c.846dup r.(?) p.(Gly283Trpfs*16)
-?/. - c.847G>C r.(?) p.(Gly283Arg)
-?/. - c.848G>C r.(?) p.(Gly283Ala)
-?/. - c.848G>C r.(?) p.(Gly283Ala)
?/. - c.865A>G r.(?) p.(Thr289Ala)
?/. - c.865A>G r.(?) p.(Thr289Ala)
+/. 10 c.937G>A r.(?) p.(Gly313Ser)
-?/. - c.937+41G>T r.(=) p.(=)
?/. - c.937+43G>A r.(=) p.(=)
?/. - c.937+66C>G r.(=) p.(=)
-?/. - c.937+91G>A r.(=) p.(=)
?/. - c.937+92T>C r.(=) p.(=)
?/. - c.937+92T>C r.(=) p.(=)
-?/. - c.937+102G>A r.(=) p.(=)
-?/. - c.961G>A r.(?) p.(Gly321Ser)
+/. 11 c.972del r.(?) p.(Met325TrpfsTer6)
+/. 11 c.972del r.(?) p.(Met325TrpfsTer6)
+/. 11 c.972dup r.(?) p.(Met325HisfsTer128)
+/. 11 c.972dup r.(?) p.(Met325HisfsTer128)
+/. - c.972dup r.(?) p.(Met325HisfsTer128)
+/. - c.972dup r.(?) p.(Met325HisfsTer128)
+/. - c.972dup r.(?) p.(Met325HisfsTer128)
+/. - c.973_974insC r.(?) p.(Met325ThrfsTer128)
-?/. - c.1029T>C r.(?) p.(Pro343=)
+/. - c.1034_1035insCTGGGCCC r.(?) p.(Ser346TrpfsTer15)
-?/. - c.1167G>A r.(?) p.(Ala389=)
-?/. - c.1167G>A r.(?) p.(Ala389=)
+/. 13 c.1189del r.(?) p.(Gln397SerfsTer2)
+/. 13 c.1189del r.(?) p.(Gln397SerfsTer2)
+/. 13 c.1189del r.(?) p.(Gln397SerfsTer2)
+/. - c.1189del r.(?) p.(Gln397SerfsTer2)
+/. - c.1189del r.(?) p.(Gln397SerfsTer2)
+/. - c.1189del r.(?) p.(Gln397SerfsTer2)
?/. - c.1268C>T r.(?) p.(Pro423Leu)
-?/. - c.1383C>T r.(?) p.(Pro461=)
?/. - c.1384G>A r.(?) p.(Gly462Arg)
+/. 15 c.1423_1428del r.(?) p.(Lys475_Arg476del)
-/. - c.1472C>G r.(?) p.(Pro491Arg)
-?/. - c.1531C>A r.(?) p.(Arg511=)
-/. - c.1532+5G>A r.spl? p.?
-/. - c.1532+5G>A r.spl? p.?
-?/. - c.1533-5G>A r.spl? p.?
-?/. - c.1533-5G>C r.spl? p.?
-/. - c.1533-5G>C r.spl? p.?
?/. - c.1568T>A r.(?) p.(Val523Glu)
-?/. - c.1698G>A r.(?) p.(Ser566=)
?/. - c.1718C>G r.(?) p.(Pro573Arg)
-/. - c.1743+9T>C r.(=) p.(=)
-?/. - c.1744-8T>C r.(=) p.(=)
+/. 4 c.1744-2A>C r.spl p.?
?/. - c.1796C>T r.(?) p.(Thr599Met)
-/. - c.1808A>G r.(?) p.(Gln603Arg)
?/. - c.1888G>A r.(?) p.(Val630Ile)
-?/. - c.1888G>A r.(?) p.(Val630Ile)
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