Transcript #00015840 (NM_000489.3, ATRX gene)

Transcript name Manually created transcript.
Gene name ATRX (alpha thalassemia/mental retardation syndrome X-linked)
Chromosome X
Transcript - NCBI ID NM_000489.3
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

33 entries on 1 page. Showing entries 1 - 33.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.288A>G 288 r.(?) p.(=) - coding-synonymous -
./. - c.370+35G>A 370 r.(=) p.(=) - intron 35
./. - c.595-36T>C 595 r.(=) p.(=) - intron 36
./. - c.595-36T>C 595 r.(=) p.(=) - intron 36
./. - c.595-36T>C 595 r.(=) p.(=) - intron 36
./. - c.595-36T>C 595 r.(=) p.(=) - intron 36
./. - c.595-36T>C 595 r.(=) p.(=) - intron 36
./. - c.595-36T>C 595 r.(=) p.(=) - intron 36
./. - c.595-36T>C 595 r.(=) p.(=) - intron 36
./. - c.595-36T>C 595 r.(=) p.(=) - intron 36
./. - c.595-36T>C 595 r.(=) p.(=) - intron 36
./. - c.595-36T>C 595 r.(=) p.(=) - intron 36
./. - c.595-36T>C 595 r.(=) p.(=) - intron 36
./. - c.595-36T>C 595 r.(=) p.(=) - intron 36
./. - c.1521C>A 1521 r.(?) p.(=) - coding-synonymous -
./. - c.2466A>C 2466 r.(?) p.(Glu822Asp) - missense -
./. - c.2785C>G 2785 r.(?) p.(Gln929Glu) - missense -
./. - c.2785C>G 2785 r.(?) p.(Gln929Glu) - missense -
./. - c.2785C>G 2785 r.(?) p.(Gln929Glu) - missense -
./. - c.2785C>G 2785 r.(?) p.(Gln929Glu) - missense -
./. - c.2785C>G 2785 r.(?) p.(Gln929Glu) - missense -
./. - c.2785C>G 2785 r.(?) p.(Gln929Glu) - missense -
./. - c.2785C>G 2785 r.(?) p.(Gln929Glu) - missense -
./. - c.2785C>G 2785 r.(?) p.(Gln929Glu) - missense -
./. - c.2785C>G 2785 r.(?) p.(Gln929Glu) - missense -
./. - c.2785C>G 2785 r.(?) p.(Gln929Glu) - missense -
./. - c.2785C>G 2785 r.(?) p.(Gln929Glu) - missense -
./. - c.2785C>G 2785 r.(?) p.(Gln929Glu) - missense -
./. - c.3541G>C 3541 r.(?) p.(Val1181Leu) - missense -
./. - c.4659T>C 4659 r.(?) p.(=) - coding-synonymous -
./. - c.4659T>C 4659 r.(?) p.(=) - coding-synonymous -
./. - c.5787-24G>T 5787 r.(=) p.(=) - intron 24
./. - c.6849+31G>T 6849 r.(=) p.(=) - intron 31
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