Transcript #00000301 (NM_021949.3, ATP2B3 gene)

Transcript name transcript variant 1
Gene name ATP2B3 (ATPase, Ca++ transporting, plasma membrane 3)
Chromosome X
Transcript - NCBI ID NM_021949.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_068768.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -


Variants

160 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-90900_*764445dup r.0? p.0?
?/. - c.83G>C r.(?) p.(Gly28Ala)
?/. - c.172G>A r.(?) p.(Gly58Arg)
-?/. - c.214G>A r.(?) p.(Ala72Thr)
-?/. - c.324C>T r.(?) p.(Asp108=)
-?/. - c.384G>A r.(?) p.(Ala128=)
-?/. - c.387G>A r.(?) p.(Pro129=)
-/. - c.406+20G>A r.(=) p.(=)
-/. - c.407-6G>A r.(=) p.(=)
-?/. - c.430G>A r.(?) p.(Ala144Thr)
?/. - c.588G>A r.(?) p.(=)
-?/. - c.588G>A r.(?) p.(Thr196=)
-?/. - c.630G>A r.(?) p.(Ala210=)
?/. - c.657C>A r.(?) p.(Val219=)
?/. - c.664+41G>A r.(=) p.(=)
?/. - c.664+41G>A r.(=) p.(=)
?/. - c.664+120_664+122del r.(=) p.(=)
?/. - c.664+120_664+122del r.(=) p.(=)
?/. - c.664+121_664+123del r.(=) p.(=)
?/. - c.664+121_664+123del r.(=) p.(=)
?/. - c.665-155del r.(=) p.(=)
?/. - c.665-155del r.(=) p.(=)
?/. - c.665-149del r.(=) p.(=)
?/. - c.665-149del r.(=) p.(=)
?/. - c.665-116A>G r.(=) p.(=)
?/. - c.665-116A>G r.(=) p.(=)
?/. - c.694A>C r.(?) p.(Ile232Leu)
-?/. - c.694A>C r.(?) p.(Ile232Leu)
-?/. - c.694A>C r.(?) p.(Ile232Leu)
-?/. - c.720C>T r.(?) p.(Asp240=)
?/. - c.781C>G r.(?) p.(Leu261Val)
?/. - c.790+17G>C r.(=) p.(=)
-/. - c.790+17G>C r.(=) p.(=)
-/. - c.790+17G>C r.(=) p.(=)
?/. - c.790+17G>C r.(=) p.(=)
?/. - c.790+214G>A r.(=) p.(=)
?/. - c.790+214G>A r.(=) p.(=)
-?/. - c.886G>A r.(?) p.(Gly296Arg)
?/. - c.1014G>A r.(?) p.(=)
-?/. - c.1053C>G r.(?) p.(Asn351Lys)
?/. - c.1090C>A r.(?) p.(Leu364Ile)
-?/. - c.1099C>T r.(?) p.(Leu367=)
-?/. - c.1146C>T r.(?) p.(Thr382=)
-?/. - c.1233A>G r.(?) p.(Val411=)
?/. - c.1473A>G r.(?) p.(=)
?/. - c.1473A>G r.(?) p.(=)
-/. - c.1473A>G r.(?) p.(Gly491=)
?/. - c.1473A>G r.(?) p.(=)
-/. - c.1473A>G r.(?) p.(Gly491=)
-?/. - c.1571C>G r.(?) p.(Thr524Ser)
-?/. - c.1581+3G>A r.spl? p.?
-?/. - c.1681G>A r.(?) p.(Val561Met)
?/. - c.1686C>G r.(?) p.(=)
?/. - c.1687G>A r.(?) p.(Glu563Lys)
-?/. - c.1763G>A r.(?) p.(Arg588His)
-?/. - c.1763G>A r.(?) p.(Arg588His)
?/. - c.1823+142C>T r.(=) p.(=)
?/. - c.1823+142C>T r.(=) p.(=)
?/. - c.1823+359T>C r.(=) p.(=)
?/. - c.1824-58G>A r.(=) p.(=)
?/. - c.1824-58G>A r.(=) p.(=)
-?/. - c.1852G>A r.(?) p.(Glu618Lys)
-?/. - c.1852G>A r.(?) p.(Glu618Lys)
?/. - c.1859G>A r.(?) p.(Arg620Gln)
?/. - c.1921G>A r.(?) p.(Asp641Asn)
-?/. - c.1921G>A r.(?) p.(Asp641Asn)
?/. - c.1930C>T r.(?) p.(Arg644Cys)
-?/. - c.1944C>T r.(?) p.(Ile648=)
?/. - c.1945G>A r.(?) p.(Ala649Thr)
-?/. - c.1967G>A r.(?) p.(Gly656Asp)
?/. - c.2029G>A r.(?) p.(Val677Met)
?/. - c.2058+163G>T r.(=) p.(=)
?/. - c.2058+163G>T r.(=) p.(=)
-?/. - c.2075G>A r.(?) p.(Arg692Gln)
?/. - c.2158G>A r.(?) p.(Gly720Ser)
-?/. - c.2211C>T r.(?) p.(Asn737=)
?/. - c.2222G>A r.(?) p.(Arg741His)
?/. - c.2326+11C>T r.(=) p.(=)
-/. - c.2326+11C>T r.(=) p.(=)
-/. - c.2326+11C>T r.(=) p.(=)
?/. - c.2326+11C>T r.(=) p.(=)
-/. - c.2326+20C>T r.(=) p.(=)
?/. - c.2434-229_2434-228insGCC r.(=) p.(=)
-?/. - c.2434-7C>T r.(=) p.(=)
-?/. - c.2505C>T r.(?) p.(Ile835=)
?/. - c.2519T>C r.(?) p.(Met840Thr)
?/. - c.2592G>C r.(?) p.(=)
?/. - c.2592G>C r.(?) p.(=)
-/. - c.2592G>C r.(?) p.(Val864=)
-/. - c.2592G>C r.(?) p.(Val864=)
?/. - c.2592G>C r.(?) p.(=)
?/. - c.2738C>T r.(?) p.(Pro913Leu)
?/. - c.2767C>T r.(?) p.(Arg923Cys)
-?/. - c.2812G>A r.(?) p.(Ala938Thr)
?/. - c.2839+14G>T r.(=) p.(=)
-/. - c.2839+14G>T r.(=) p.(=)
-/. - c.2839+14G>T r.(=) p.(=)
?/. - c.2839+14G>T r.(=) p.(=)
?/. - c.2839+33A>G r.(=) p.(=)
?/. - c.2839+33A>G r.(=) p.(=)
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