Transcript #00001687 (NM_001142864.2, PIEZO1 gene)

Transcript name piezo-type mechanosensitive ion channel component 1
Gene name PIEZO1 (piezo-type mechanosensitive ion channel component 1)
Chromosome 16
Transcript - NCBI ID NM_001142864.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001136336.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 13:46:06 +02:00 (CEST)
Date last edited N/A


Variants

546 entries on 6 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.63T>G r.(?) p.(Ala21=)
-?/. - c.64+17C>T r.(=) p.(=)
-?/. 1i c.64+8356C>T r.(?) p.(=)
-?/. - c.65-17C>G r.(=) p.(=)
?/. - c.85G>A r.(?) p.(Gly29Arg)
-/. - c.132C>T r.(?) p.(Phe44=)
?/. - c.173G>A r.(?) p.(Arg58His)
-/. - c.248T>C r.(?) p.(Ile83Thr)
-?/. - c.263A>G r.(?) p.(Asp88Gly)
-?/. - c.263A>G r.(?) p.(Asp88Gly)
-?/. - c.283+7C>T r.(=) p.(=)
-?/. - c.283+11G>C r.(=) p.(=)
-?/. - c.284-4G>A r.spl? p.?
+/. - c.307C>T r.(?) p.(Arg103Ter)
-?/. - c.363G>C r.(?) p.(Leu121=)
?/. - c.376C>G r.(?) p.(Leu126Val)
-/. - c.455C>T r.(?) p.(Pro152Leu)
-/. - c.465+8C>T r.(=) p.(=)
-/. - c.555C>T r.(?) p.(Ala185=)
-?/. - c.566G>A r.(?) p.(Arg189Gln)
-/. - c.588G>T r.(?) p.(Leu196=)
-?/. - c.588G>T r.(?) p.(Leu196=)
?/. - c.590_599del r.(?) p.(Val197Glyfs*6)
-?/. - c.601C>A r.(?) p.(Arg201=)
?/. - c.608T>C r.(?) p.(Leu203Pro)
-?/. - c.627A>G r.(?) p.(Ala209=)
-/. - c.627A>G r.(?) p.(Ala209=)
-?/. - c.635-50G>A r.(?) p.(?)
-/. - c.635-8C>T r.(=) p.(=)
-?/. - c.635-4G>A r.spl? p.?
-?/. - c.718A>G r.(?) p.(Ile240Val)
-?/. - c.747C>T r.(?) p.(Cys249=)
-/. - c.749T>C r.(?) p.(Val250Ala)
-?/. - c.751G>A r.(?) p.(Ala251Thr)
-?/. - c.757G>A r.(?) p.(Gly253Arg)
?/. - c.757G>A r.(?) p.(Gly253Arg)
?/. - c.812C>T r.(?) p.(Ala271Val)
-?/. - c.835G>A r.(?) p.(Gly279Ser)
-/. - c.848+17C>T r.(=) p.(=)
-?/. - c.849-10C>T r.(=) p.(=)
-?/. - c.919G>A r.(?) p.(Gly307Ser)
-?/. - c.954C>T r.(?) p.(Val318=)
-?/. - c.954C>T r.(?) p.(Val318=)
-?/. - c.998G>A r.(?) p.(Arg333His)
-/. - c.998G>A r.(?) p.(Arg333His)
-?/. - c.998G>A r.(?) p.(Arg333His)
-?/. - c.999C>T r.(?) p.(Arg333=)
-?/. - c.1001C>T r.(?) p.(Ala334Val)
-?/. - c.1009C>T r.(?) p.(Pro337Ser)
-?/. - c.1009C>T r.(?) p.(Pro337Ser)
-?/. - c.1009C>T r.(?) p.(Pro337Ser)
-?/. - c.1013C>A r.(?) p.(Ser338Tyr)
-/. - c.1013C>A r.(?) p.(Ser338Tyr)
-?/. - c.1022G>T r.(?) p.(Arg341Met)
-?/. - c.1049C>T r.(?) p.(Ala350Val)
-?/. - c.1072C>T r.(?) p.(Leu358=)
?/. - c.1075G>A r.(?) p.(Asp359Asn)
-?/. - c.1093C>T r.(?) p.(Arg365Trp)
?/. - c.1107+1G>C r.spl? p.?
-?/. - c.1123G>A r.(?) p.(Ala375Thr)
-?/. - c.1132A>G r.(?) p.(Thr378Ala)
-/. - c.1141_1143del r.(?) p.(Asp381del)
?/. - c.1163T>C r.(?) p.(Leu388Pro)
-/. - c.1180G>C r.(?) p.(Val394Leu)
-?/. - c.1187G>A r.(?) p.(Arg396Gln)
-?/. - c.1188G>A r.(?) p.(Arg396=)
-?/. - c.1195+9C>T r.(=) p.(=)
-/. - c.1196-17G>A r.(=) p.(=)
-?/. - c.1196-10C>T r.(=) p.(=)
-?/. - c.1199G>A r.(?) p.(Arg400Gln)
-/. - c.1219A>G r.(?) p.(Arg407Gly)
?/. - c.1232C>T r.(?) p.(Pro411Leu)
-?/. - c.1251C>T r.(?) p.(His417=)
-?/. - c.1251C>T r.(?) p.(His417=)
?/. - c.1277G>A r.(?) p.(Cys426Tyr)
-?/. - c.1281G>A r.(?) p.(Ala427=)
-/. - c.1297-16C>T r.(=) p.(=)
-/. - c.1297-14T>C r.(=) p.(=)
-?/. - c.1297-6G>A r.(=) p.(=)
-/. - c.1365G>A r.(?) p.(Thr455=)
-/. - c.1365G>A r.(?) p.(Thr455=)
?/. - c.1373G>A r.(?) p.(Ser458Asn)
-?/. - c.1401G>A r.(?) p.(Ser467=)
?/. - c.1481C>A r.(?) p.(Thr494Asn)
-?/. - c.1495G>A r.(?) p.(Val499Ile)
-?/. - c.1495G>A r.(?) p.(Val499Ile)
-?/. - c.1495G>A r.(?) p.(Val499Ile)
?/. - c.1496T>G r.(?) p.(Val499Gly)
-?/. - c.1527C>A r.(?) p.(Thr509=)
-/. - c.1527C>A r.(?) p.(Thr509=)
?/. - c.1534C>A r.(?) p.(Pro512Thr)
?/. - c.1534C>T r.(?) p.(Pro512Ser)
?/. - c.1534C>T r.(?) p.(Pro512Ser)
-/. - c.1540C>T r.(?) p.(Leu514=)
-/. - c.1557+16C>G r.(=) p.(=)
?/. - c.1591C>T r.(?) p.(Arg531Cys)
?/. - c.1591C>T r.(?) p.(Arg531Cys)
-?/. - c.1641G>A r.(?) p.(=)
-?/. - c.1657G>A r.(?) p.(Val553Met)
+?/. 13i c.1669+1G>A r.spl? p.?
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