All variants in the TMEM151A gene

Information The variants shown are described using the NM_153266.4 transcript reference sequence.

38 entries on 1 page. Showing entries 1 - 38.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Type     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Variant remarks     

ClassClinical     

Owner     
+?/+? 1 c.7G>T r.7g>u p.E3* Substitution g.151G>T GenBank TMEM151A_000007 - - - Yulan Chen
+?/+? 2 c.128G>A r.128g>a p.W43* Substitution g.2505G>A GenBank TMEM151A_000128 - identified in one PKD family (Mov Disord. 2022;37(3):545-552) - Yulan Chen
+?/+? 2 c.129G>A c.129g>a p.W43* Substitution g.2506G>A - TMEM151A_001276 1/521 patients identified in one sporadic PKD patient(Mov Disord. 2022;37(3):545-552) - Yulan Chen
?/? 2 c.133T>C c.133u>c p.C45R Substitution g.2510T>C - TMEM151A_001278 1/521 patients identified in one sporadic PKD patient(Mov Disord. 2022;37(3):545-552) - Yulan Chen
?/? 2 c.133T>G r.133u>g p.C45G Substitution g.2510T>G - TMEM151A_001277 1/521 patients identified in one sporadic PKD patient(Mov Disord. 2022;37(3):545-552) - Yulan Chen
+/+ 2 c.140T>C r.140u>c p.L47P Substitution g.2517T>C GenBank TMEM151A_000140 2/167 patients identified in sporadic patients (Cell Discov. 2021;7(1):83.Mov Disord. 2022;37(3):608-613) - Yulan Chen
+/+ 2 c.142_153del r.142_153del p.48_51delLTLL Deletion g.2519_2530del GenBank TMEM151A_000142 1/36 patients identified in one sporadic PKD patient - Yulan Chen
+?/+? 2 c.203C>T r.203c>u p.P68L Substitution g.2580C>T GenBank TMEM151A_000203 1/521 patients identified in one PKD family (Mov Disord. 2022;37(3):545-552.) - Yulan Chen
+?/+? 2 c.375C>A r.375c>a p.C125* Substitution g.2752C>A GenBank TMEM151A_001272 - reported by different research groups (Cell Discov. 2021;7(1):83.Mov Disord. 2022;37(3):545-552. ) - Yulan Chen
?/+? 2 c.469C>T r.469c>u p.H157Y Substitution g.2846C>T GenBank TMEM151A_000469 - identified in a PKD family(Mov Disord. 2022;37(3):608-613) - Yulan Chen
?/? 2 c.497C>A r.497c>a p.T166K Substitution g.2874C>A - TMEM151A_001279 1/521 patients identified in one sporadic PKD patient(Mov Disord. 2022;37(3):545-552) - Yulan Chen
+?/+? 2 c.499C>T r.499c>u p.R167C Substitution g.2876C>T - TMEM151A_000499 1/521 patients identified in one PKD family with incomplete penetrance (Mov Disord. 2022;37(3):545-552.) - Yulan Chen
+?/+? 2 c.578T>C r.578u>c p.F193S Substitution g.2955T>C - TMEM151A_001274 1/521 patients identified in one PKD family(Mov Disord. 2022;37(3):545-552) - Yulan Chen
+?/+? 2 c.623_624insA r.623_624insa p.L210Afs*136 Insertion g.3000_3001insA GenBank TMEM151A_000623 1/36 patients Identified in one sporadic patient(Cell Discov. 2021;7(1):83.) - Yulan Chen
+?/+? 2 c.647C>A r.647c>a p.T216K Substitution g.3024C>A GenBank TMEM151A_000647 1/131 patients identified in one sporadic patient and the variant was drived from de novo (Mov Disord. 2022;37(3):608-613) - Yulan Chen
+?/+? 2 c.704A>G r.704a>g Y235C Substitution g.3081A>G - TMEM151A_000704 1/521 patients identified in one PKD family (Mov Disord. 2022;37(3):545-552) - Yulan Chen
?/+? 2 c.712C>T r.712c>u p.Q238* Substitution g.3089C>T - TMEM151A_001280 1/521 patients identified in one sporadic PKD patient(Mov Disord. 2022;37(3):545-552) - Yulan Chen
?/+? 2 c.739G>T r.739g>u p.E247* Substitution g.3116G>T GenBank TMEM151A_000898 - also identified in asymptomatic parents, possible incomplete penetrance.(Cell Discov. 2021;7(1):83;Mov Disord. 2022;37(3):608-613) - Yulan Chen
+/+ 2 c.758T>C r.758u>c p.L253P Substitution g.3135T>C GenBank TMEM151A_000758 1/36 patients identified in one PKD family (Cell Discov. 2021;7(1):83) - Yulan Chen
?/? 2 c.769G>A r.769g>a p.E257K Substitution g.3146G>A - TMEM151A_001281 1/521 patients identified in one sporadic PKD patient(Mov Disord. 2022;37(3):545-552) - Yulan Chen
+?/+? 2 c.791T>C c.791u>c p.V264A Substitution g.3168T>C - TMEM151A_001275 1/521 patients identified in one PKD family(Mov Disord. 2022;37(3):545-552) - Yulan Chen
?/? 2 c.815T>C r.815u>c p.V272A Substitution g.3192T>C - TMEM151A_000815 1/521 patients identified in one sporadic PKD patient(Mov Disord. 2022;37(3):545-552) - Yulan Chen
?/? 2 c.827C>G r.827c>g p.P276R Substitution g.3204C>G - TMEM151A_001282 1/521 patients identified in one sporadic PKD patient(Mov Disord. 2022;37(3):545-552) - Yulan Chen
+?/+? 2 c.827C>T r.827c>u p.P276L Substitution g.3204C>T GenBank TMEM151A_000827 1/131 patients identified in one sporadic patient (Mov Disord. 2022;37(3):608-613) - Yulan Chen
?/? 2 c.845A>G r.845a>g p.Y282C Substitution g.3222A>G - TMEM151A_001283 1/521 patients identified in one sporadic PKD patient(Mov Disord. 2022;37(3):545-552) - Yulan Chen
+/+ 2 c.863T>C r.863u>c p.F288S Substitution g.3240T>C GenBank TMEM151A_000863 - - - Yulan Chen
+/+ 2 c.889T>A r.889u>a p.S297T Substitution g.3266T>A GenBank TMEM151A_000889 1/36 patients identified in one sporadic PKD patient(Cell Discov. 2021;7(1):83) - Yulan Chen
+?/+? 2 c.897_912del r.897_912del p.L300Pfs*118 Deletion g.3274_3289del GenBank TMEM151A_000897 - reported to have founder effect, multiple affected indenpendent individuals (Cell Discov. 2021;7(1):83. Mov Disord. 2022;37(3):641-643.) - Yulan Chen
?/? 2 c.928C>T r.928c>u p.H310Y Substitution g.3305C>T - TMEM151A_000928 1/521 patients identified in one sporadic PKD patient(Mov Disord. 2022;37(3):545-552) - Yulan Chen
?/? 2 c.955T>C r.955u>c p.F319L Deletion g.3332T>C - TMEM151A_001284 1/521 patients identified in one sporadic PKD patient(Mov Disord. 2022;37(3):545-552) - Yulan Chen
?/+? 2 c.1043G>A r.1043g>a p.W348* Substitution g.3420G>A - TMEM151A_001285 1/521 patients identified in one sporadic PKD patient(Mov Disord. 2022;37(3):545-552) - Yulan Chen
?/? 2 c.1051T>C r.1051u>c p.C351R Substitution g.3428T>C - TMEM151A_001051 1/521 patients identified in one sporadic PKD patient(Mov Disord. 2022;37(3):545-552) - Yulan Chen
?/? 2 c.1073C>T r.1073c>u p.P358L Substitution g.3450C>T - TMEM151A_001286 1/521 patients identified in one sporadic PKD patient(Mov Disord. 2022;37(3):545-552) - Yulan Chen
?/? 2 c.1081T>C r.1081u>c p.S361P Substitution g.3458T>C - TMEM151A_001287 1/521 patients identified in one sporadic PKD patient(Mov Disord. 2022;37(3):545-552) - Yulan Chen
?/? 2 c.1270G>A r.1270g>a p.G424R Substitution g.3647G>A GenBank TMEM151A_001270 1/131 patients identified in one sporadic PKD patient (Mov Disord. 2022;37(3):608-613) - Yulan Chen
+?/+? 1 c.1275_1276insG r.1275_1276insg p.P426Afs*19 Substitution g.3652_3653insG GenBank TMEM151A_001271 - identified in a PKD family with autosomal dominant inheritance - Yulan Chen
?/+? 2 c.1330G>T r.1330g>u p.E444* Substitution g.3707G>T - TMEM151A_001330 1/521 patients identified in one sporadic PKD patient(Mov Disord. 2022;37(3):545-552) - Yulan Chen
-?/-? 2 c.1382A>C r.1382a>c p.Q461P Substitution g.3759A>C GenBank TMEM151A_001273 - one PKD patient was detected to have compound heterozygous variants in TMEM151A (c.469C>T and c.1382A>C). And the variant c.1382A>C was inherited from his asymptomatic father ,while the variant c.469C>T was inherited from his mother, who also had PKD.(Mov Disord. 2022;37(3):608-613) - Yulan Chen
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