Transcript #00003116 (NM_020632.2, ATP6V0A4 gene)

Transcript name transcript variant 1
Gene name ATP6V0A4 (ATPase, H+ transporting, lysosomal V0 subunit a4)
Chromosome 7
Transcript - NCBI ID NM_020632.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_065683.2
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

64 entries on 1 page. Showing entries 1 - 64.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.5T>C r.(?) p.(Val2Ala)
+/- 3 c.5T>C r.(?) p.(Val2Ala)
-/- 3 c.5T>C r.(?) p.(Val2Ala)
-/. - c.5T>C r.(?) p.(Val2Ala)
+/. - c.16C>T r.(?) p.(Arg6Ter)
+/. 3 c.105del r.(?) p.(Gln36Serfs*5)
?/. - c.196C>T r.(?) p.(Arg66Cys)
-/. - c.196+24_196+25del r.(=) p.(=)
-/. - c.196+25del r.(=) p.(=)
-/. - c.292-42A>G r.(=) p.(=)
+/. 5i c.292-1G>A r.spl p.?
+/. - c.292-1G>A r.spl? p.?
+/. - c.338del r.(?) p.(Asn113Thrfs*5)
-/. - c.417+14G>C r.(=) p.(=)
-/. - c.417+14G>C r.(=) p.(=)
+?/. - c.620dup r.(?) p.(Leu208Serfs*33)
+/. - c.639+1G>A r.spl? p.?
-?/. - c.816+19C>T r.(=) p.(=)
+/. 11 c.(829del) r.(?) p.(Thr277Glnfs*26)
?/. - c.863C>A r.(?) p.(Ala288Asp)
-?/. - c.1002T>C r.(?) p.(Arg334=)
-/. - c.1030-14T>A r.(=) p.(=)
-/. - c.1030-5del r.spl? p.?
-/. - c.1030-5del r.spl? p.?
-/. - c.1030-5del r.spl? p.?
?/. - c.1030-5del r.spl p.(?)
-?/. - c.1030-5dup r.spl? p.?
-/. - c.1033C>A r.(?) p.(Leu345Ile)
+?/. - c.1180G>A r.(?) p.(Ala394Thr)
+/. - c.1185del r.(?) p.(Tyr396ThrfsTer12)
?/. - c.1345C>T r.(?) p.(Arg449Cys)
+?/. - c.1346G>A r.(?) p.(Arg449His)
+/. - c.1475G>A r.(?) p.(Trp492Ter)
+/. - c.1478+2T>G r.spl? p.?
+/. - c.1478+2T>G r.spl? p.?
-/. - c.1478+17A>G r.(=) p.(=)
-/. - c.1478+17A>G r.(=) p.(=)
-?/. - c.1498A>G r.(?) p.(Ser500Gly)
-/. - c.1557G>A r.(?) p.(Pro519=)
+/. 15 c.1571C>T r.(?) p.(Pro524Leu)
-?/. - c.1641G>A r.(?) p.(Leu547=)
-/. 16 c.1662C>T r.(=) p.(Phe554=)
-/. - c.1662C>T r.(?) p.(Phe554=)
-/. - c.1662C>T r.(?) p.(Phe554=)
+/. 16i c.1691+1G>A r.spl p.?
+/. - c.1691+1G>A r.spl? p.?
+/. 17 c.1739T>C r.(?) p.(Met580Thr)
-/. - c.1739T>C r.(?) p.(Met580Thr)
-/. - c.1812T>C r.(?) p.(His604=)
-/. 17 c.1812T>C r.(=) p.(His604=)
-/. - c.1812T>C r.(?) p.(His604=)
-/. - c.1888G>A r.(?) p.(Ala630Thr)
-?/. - c.1908+24_1908+25del r.(=) p.(=)
-?/. - c.1908+25del r.(=) p.(=)
-/. - c.1908+25dup r.(=) p.(=)
-/. - c.2035G>T r.(?) p.(Asp679Tyr)
-?/. - c.2113G>A r.(?) p.(Gly705Arg)
-?/. - c.2140-9G>A r.(=) p.(=)
-?/. - c.2140-9G>A r.(=) p.(=)
+/. 20 c.2257C>T r.(spl?) p.(Gln753*?)
-?/. - c.2306C>T r.(?) p.(Thr769Met)
-?/. - c.2412C>T r.(?) p.(His804=)
+/. - c.2419C>T r.(?) p.(Arg807Ter)
+/. 22 c.2458G>A r.(?) p.(Gly820Arg)
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