Transcript #00015841 (NM_138270.2, ATRX gene)

Transcript name Manually created transcript.
Gene name ATRX (alpha thalassemia/mental retardation syndrome X-linked)
Chromosome X
Transcript - NCBI ID NM_138270.2
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.481-36T>C 481 r.(=) p.(=) - intron 36
./. - c.481-36T>C 481 r.(=) p.(=) - intron 36
./. - c.481-36T>C 481 r.(=) p.(=) - intron 36
./. - c.481-36T>C 481 r.(=) p.(=) - intron 36
./. - c.481-36T>C 481 r.(=) p.(=) - intron 36
./. - c.481-36T>C 481 r.(=) p.(=) - intron 36
./. - c.481-36T>C 481 r.(=) p.(=) - intron 36
./. - c.481-36T>C 481 r.(=) p.(=) - intron 36
./. - c.481-36T>C 481 r.(=) p.(=) - intron 36
./. - c.481-36T>C 481 r.(=) p.(=) - intron 36
./. - c.481-36T>C 481 r.(=) p.(=) - intron 36
./. - c.481-36T>C 481 r.(=) p.(=) - intron 36
./. - c.1407C>A 1407 r.(?) p.(=) - coding-synonymous -
./. - c.2352A>C 2352 r.(?) p.(Glu784Asp) - missense -
./. - c.2671C>G 2671 r.(?) p.(Gln891Glu) - missense -
./. - c.2671C>G 2671 r.(?) p.(Gln891Glu) - missense -
./. - c.2671C>G 2671 r.(?) p.(Gln891Glu) - missense -
./. - c.2671C>G 2671 r.(?) p.(Gln891Glu) - missense -
./. - c.2671C>G 2671 r.(?) p.(Gln891Glu) - missense -
./. - c.2671C>G 2671 r.(?) p.(Gln891Glu) - missense -
./. - c.2671C>G 2671 r.(?) p.(Gln891Glu) - missense -
./. - c.2671C>G 2671 r.(?) p.(Gln891Glu) - missense -
./. - c.2671C>G 2671 r.(?) p.(Gln891Glu) - missense -
./. - c.2671C>G 2671 r.(?) p.(Gln891Glu) - missense -
./. - c.2671C>G 2671 r.(?) p.(Gln891Glu) - missense -
./. - c.2671C>G 2671 r.(?) p.(Gln891Glu) - missense -
./. - c.3427G>C 3427 r.(?) p.(Val1143Leu) - missense -
./. - c.4545T>C 4545 r.(?) p.(=) - coding-synonymous -
./. - c.4545T>C 4545 r.(?) p.(=) - coding-synonymous -
./. - c.5673-24G>T 5673 r.(=) p.(=) - intron 24
./. - c.6735+31G>T 6735 r.(=) p.(=) - intron 31
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