Transcript #00025423 (NM_000081.3, LYST gene)

Transcript name transcript variant 1
Gene name LYST (lysosomal trafficking regulator)
Chromosome 1
Transcript - NCBI ID NM_000081.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000072.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2019-07-17 13:19:10 +02:00 (CEST)
Date last edited N/A


Variants

388 entries on 4 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-98+5A>C r.spl? p.?
-?/. - c.-97-5T>G r.spl? p.?
-/. - c.-7-19del r.(=) p.(=)
-/. - c.-7-16A>G r.(=) p.(=)
-?/. - c.9C>T r.(?) p.(Thr3=)
?/. - c.18C>G r.(?) p.(Asn6Lys)
?/. - c.115A>G r.(?) p.(Met39Val)
?/. - c.118dup r.(?) p.(Ala40Glyfs*24)
?/. - c.122C>A r.(?) p.(Thr41Asn)
-?/. - c.143A>G r.(?) p.(His48Arg)
-?/. - c.143A>G r.(?) p.(His48Arg)
-/. - c.153A>C r.(?) p.(Gly51=)
-?/. - c.192+8T>G r.(=) p.(=)
?/. 4 c.281C>T r.(?) p.(Thr94Ile)
-?/. - c.285T>C r.(?) p.(Asp95=)
-/. - c.348A>G r.(?) p.(Arg116=)
-?/. - c.368A>G r.(?) p.(His123Arg)
?/. - c.422G>A r.(?) p.(Arg141Gln)
-?/. - c.553C>T r.(?) p.(Pro185Ser)
-/. - c.574T>G r.(?) p.(Leu192Val)
-/. - c.574T>G r.(?) p.(Leu192Val)
-?/. - c.595G>A r.(?) p.(Asp199Asn)
-?/. - c.597C>G r.(?) p.(Asp199Glu)
?/. - c.646C>T r.(?) p.(Pro216Ser)
-?/. - c.646C>T r.(?) p.(Pro216Ser)
-?/. - c.692A>G r.(?) p.(Gln231Arg)
+/. - c.949G>A r.(?) p.(Glu317Lys)
?/. - c.949G>A r.(?) p.(Glu317Lys)
?/. - c.986G>A r.(?) p.(Arg329Gln)
?/. - c.1296G>T r.(?) p.(Leu432Phe)
-?/. - c.1384C>T r.(?) p.(Pro462Ser)
-?/. - c.1384C>T r.(?) p.(Pro462Ser)
+/. 5 c.1463C>G r.(?) p.(Ser488Ter)
-?/. - c.1508G>A r.(?) p.(Arg503Gln)
?/. - c.1615G>A r.(?) p.(Gly539Arg)
-?/. - c.1686G>C r.(?) p.(Gln562His)
+?/. - c.1686G>C r.(?) p.(Gln562His)
-?/. - c.1686G>C r.(?) p.(Gln562His)
-?/. - c.1722A>G r.(?) p.(Leu574=)
?/. - c.1814A>C r.(?) p.(Lys605Thr)
?/. - c.1829A>T r.(?) p.(His610Leu)
-?/. - c.1908T>C r.(?) p.(Ala636=)
?/. - c.1940T>G r.(?) p.(Leu647Arg)
-?/. - c.1975T>C r.(?) p.(Cys659Arg)
?/. - c.2258G>A r.(?) p.(Ser753Asn)
-?/. - c.2258G>A r.(?) p.(Ser753Asn)
-?/. - c.2313G>A r.(?) p.(Gln771=)
-?/. - c.2313G>A r.(?) p.(Gln771=)
-/. - c.2313G>A r.(?) p.(Gln771=)
-?/. - c.2363+4T>C r.spl? p.?
-?/. - c.2363+4T>C r.spl? p.?
-?/. - c.2363+4T>C r.spl? p.?
?/. - c.2363+4T>C r.spl? p.?
-?/. - c.2363+7A>T r.(=) p.(=)
-/. - c.2363+10dup r.(=) p.(=)
-?/. - c.2363+10dup r.(=) p.(=)
-?/. - c.2363+10dup r.(=) p.(=)
-?/. - c.2363+17G>A r.(=) p.(=)
?/. - c.2455G>A r.(?) p.(Ala819Thr)
?/. - c.2455G>A r.(?) p.(Ala819Thr)
-?/. - c.2460T>G r.(?) p.(Phe820Leu)
-?/. - c.2610T>C r.(?) p.(Ser870=)
-?/. - c.2642C>T r.(?) p.(Ala881Val)
-?/. - c.2646T>C r.(?) p.(Tyr882=)
-?/. - c.2724C>T r.(?) p.(Cys908=)
-?/. - c.2754G>A r.(?) p.(Glu918=)
-?/. - c.2757G>A r.(?) p.(Ser919=)
-?/. - c.2757G>A r.(?) p.(Ser919=)
-?/. - c.2769A>C r.(?) p.(Ser923=)
-?/. - c.2769A>C r.(?) p.(Ser923=)
?/. - c.2839G>C r.(?) p.(Glu947Gln)
-/. - c.2908A>C r.(?) p.(Ile970Leu)
-/. - c.2946T>C r.(?) p.(Tyr982=)
-?/. - c.2946T>C r.(?) p.(Tyr982=)
-?/. - c.3030A>G r.(?) p.(Gly1010=)
-?/. - c.3030A>G r.(?) p.(Gly1010=)
-?/. - c.3031A>G r.(?) p.(Lys1011Glu)
-/. - c.3050G>A r.(?) p.(Ser1017Asn)
-/. - c.3050G>A r.(?) p.(Ser1017Asn)
-?/. - c.3083C>G r.(?) p.(Ser1028Cys)
?/. - c.3083C>G r.(?) p.(Ser1028Cys)
?/. - c.3083C>G r.(?) p.(Ser1028Cys)
?/. - c.3103A>G r.(?) p.(Lys1035Glu)
-?/. - c.3119C>G r.(?) p.(Ser1040Cys)
-?/. - c.3123G>A r.(?) p.(Leu1041=)
-?/. - c.3134G>A r.(?) p.(Ser1045Asn)
?/. - c.3137A>G r.(?) p.(Asp1046Gly)
-?/. - c.3177T>C r.(?) p.(Ala1059=)
-?/. - c.3177T>C r.(?) p.(Ala1059=)
?/. - c.3310C>T r.(?) p.(Arg1104*)
+?/. - c.3310C>T r.(?) p.(Arg1104*)
-?/. - c.3359G>T r.(?) p.(Ser1120Ile)
-?/. - c.3394-14T>C r.(=) p.(=)
-?/. - c.3394-14T>C r.(=) p.(=)
-?/. - c.3394-5C>T r.spl? p.?
-?/. - c.3507C>T r.(?) p.(Leu1169=)
-/. - c.3507C>T r.(?) p.(Leu1169=)
-?/. - c.3507C>T r.(?) p.(Leu1169=)
-?/. - c.3555+10A>G r.(=) p.(=)
?/. - c.3574_3576del r.(?) p.(Glu1192del)
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