Transcript #00000020 (NM_000053.3, ATP7B gene)

Transcript name ATPase, Cu++ transporting, beta polypeptide, transcript variant 1
Gene name ATP7B (ATPase copper transporting beta)
Chromosome 13
Transcript - NCBI ID NM_000053.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000044.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2016-07-08 14:44:23 +00:00 (UTC)
Date last edited N/A


Variants

18 entries on 1 page. Showing entries 1 - 18.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Class     
?/? 1 c.-472G>T r.(=) p.(=) VUS
?/? 1 c.-383G>T r.(=) p.(=) -
?/? 1 c.-30C>G r.(=) p.(=) VUS
+/+ 2 c.1162C>T r.(?) p.(Gln388*) pathogenic
+/+ 6 c.1877G>C r.(?) p.(Gly626Ala) likely pathogenic
+?/+? 7 c.1995G>A r.(?) p.(Met665Ile) likely pathogenic
+/+ 8 c.2128G>A r.(?) p.(Gly710Ser) -
+/+ 8 c.2129G>C r.(?) p.(Gly710Ala) pathogenic
+/+ 3 c.2332C>G r.(?) p.(Arg778Gly) pathogenic
+/+ 13 c.2906G>A r.(?) p.(Arg969Gln) pathogenic
+/+ 14 c.3061-12T>A r.(=) p.(=) -
+/+ 14 c.3207C>A r.(?) p.(His1069Gln) pathogenic
+?/+? 14 c.3243+5G>A r.spl? p.? likely benign
+/+ 16 c.3443T>C r.(?) p.(Ile1148Thr) pathogenic
+/+ 16 c.3526G>A r.(?) p.(Gly1176Arg) pathogenic
?/? 17 c.3688A>G r.(?) p.(Ile1230Val) likely pathogenic
+/+ 20 c.4051C>T r.(?) p.(Gln1351*) pathogenic
+/+ 21 c.4374_4375del r.(?) p.(Arg1459Glyfs*2) pathogenic
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