Transcript #00009603 (NM_024747.5, HPS6 gene)

Transcript name Hermansky-Pudlak syndrome 6
Gene name HPS6 (Hermansky-Pudlak syndrome 6)
Chromosome 10
Transcript - NCBI ID NM_024747.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_079023.2
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

67 entries on 1 page. Showing entries 1 - 67.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. _1_ c.-108_*236{0} r.0? p.0?
+/. _1_ c.-108_*236{0} r.0? p.0?
+/. _1_ c.-108_*236{0} r.0? p.0?
+/. _1_ c.-108_*236{0} r.0? p.0?
-/. - c.61C>A r.(?) p.(Arg21=)
+/. 1 c.62_63insCGGCG r.(?) p.(Leu22GlyfsTer33)
?/. - c.112C>G r.(?) p.(Pro38Ala)
+/. 1 c.141_143delinsG r.(?) p.(Pro49TrpfsTer126)
+/. 1 c.223C>T r.(?) p.(Gln75Ter)
+/. 1 c.238dup r.(?) p.(Asp80GlyfsTer96)
?/. - c.254C>T r.(?) p.(Pro85Leu)
+/. 1 c.275T>A r.(?) p.(Leu92Gln)
?/. - c.275T>A r.(?) p.(Leu92Gln)
-?/. - c.322G>T r.(?) p.(Val108Leu)
?/. - c.337C>T r.(?) p.(Arg113Trp)
-?/. - c.337C>T r.(?) p.(Arg113Trp)
+/. 1 c.337C>T r.(?) p.(Arg113Trp)
-/. - c.398C>T r.(?) p.(Ala133Val)
-?/. - c.398C>T r.(?) p.(Ala133Val)
+/. 1 c.455C>G r.(?) p.(Ser152Ter)
+/. 1 c.455C>G r.(?) p.(Ser152Ter)
+/. 1 c.455C>G r.(?) p.(Ser152Ter)
-?/. - c.575G>A r.(?) p.(Gly192Glu)
-/. - c.632G>C r.(?) p.(Gly211Ala)
-?/. - c.804G>T r.(?) p.(Leu268=)
+/. 1 c.815C>T r.(?) p.(Thr272Ile)
+/. 1 c.896G>C r.(?) p.(Arg299Pro)
+/. 1 c.905G>A r.(?) p.(Gly302Asp)
+/. 1 c.913C>T r.(?) p.(Gln305Ter)
-/. - c.1035G>A r.(?) p.(Arg345=)
+/. 1 c.1065dup r.(?) p.(Leu356AlafsTer11)
-/. - c.1083C>T r.(?) p.(Pro361=)
-?/. - c.1083C>T r.(?) p.(Pro361=)
+/. - c.1228_1252del r.(?) p.(Tyr410ValfsTer9)
+/. - c.1228_1252del r.(?) p.(Tyr410ValfsTer9)
+/. 1 c.1234C>T r.(?) p.(Gln412Ter)
?/. - c.1253G>T r.(?) p.(Gly418Val)
?/. - c.1273_1275del r.(?) p.(Glu425del)
?/. - c.1283A>G r.(?) p.(His428Arg)
-?/. - c.1363T>C r.(?) p.(Leu455=)
+/. 1 c.1387C>T r.(?) p.(Arg463Ter)
?/. - c.1407G>C r.(?) p.(Lys469Asn)
-?/. - c.1417G>A r.(?) p.(Val473Met)
-/. - c.1458G>A r.(?) p.(Ala486=)
-?/. - c.1458G>A r.(?) p.(Ala486=)
-/. - c.1692C>T r.(?) p.(Pro564=)
+/. 1 c.1714_1717del r.(?) p.(Leu572Alafs*40)
+/. 1 c.1714_1717del r.(?) p.(Leu572AlafsTer40)
+/. 1 c.1714_1717del r.(?) p.(Leu572AlafsTer40)
?/. - c.1778C>G r.(?) p.(Pro593Arg)
-?/. - c.1779G>A r.(?) p.(Pro593=)
-?/. - c.1782C>G r.(?) p.(Gly594=)
+/. 1 c.1819C>T r.(?) p.(Arg607Ter)
+?/. - c.1819C>T r.(?) p.(Arg607*)
+/. 1 c.1865_1866del r.(?) p.(Leu622Argfs*12)
+?/. - c.1946G>A r.(?) p.(Trp649Ter)
?/. - c.1951C>T r.(?) p.(Arg651Trp)
?/. - c.1951C>T r.(?) p.(Arg651Trp)
?/. - c.2000G>A r.(?) p.(Arg667Gln)
?/. - c.2029G>A r.(?) p.(Glu677Lys)
?/. - c.2078G>A r.(?) p.(Arg693His)
-?/. - c.2145G>C r.(?) p.(Glu715Asp)
-?/. - c.2181A>G r.(?) p.(Ala727=)
+/. 1 c.2207T>C r.(?) p.(Leu736Pro)
?/. - c.2216T>C r.(?) p.(Leu739Pro)
-/. - c.2250G>A r.(?) p.(Ser750=)
?/. - c.2260C>G r.(?) p.(Leu754Val)
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