All variants in the ATRX gene

Information The variants shown are described using the NM_000489.3 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-/. - c.4377_4379del r.(?) p.(Glu1464del) - benign g.76907796_76907798del g.77652306_77652308del ATRX(NM_000489.3):c.4377_4379del (p.(Glu1464del)), ATRX(NM_000489.5):c.4377_4379delGGA (p.E1464del), ATRX(NM_000489.6):c.4377_4379delGGA (p.E1464del) - ATRX_000172 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
-?/. - c.4377_4379del r.(?) p.(Glu1464del) - likely benign g.76907796_76907798del g.77652306_77652308del ATRX(NM_000489.3):c.4377_4379del (p.(Glu1464del)), ATRX(NM_000489.5):c.4377_4379delGGA (p.E1464del), ATRX(NM_000489.6):c.4377_4379delGGA (p.E1464del) - ATRX_000172 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
-?/. - c.4377_4379del r.(?) p.(Glu1464del) - likely benign g.76907796_76907798del - ATRX(NM_000489.3):c.4377_4379del (p.(Glu1464del)), ATRX(NM_000489.5):c.4377_4379delGGA (p.E1464del), ATRX(NM_000489.6):c.4377_4379delGGA (p.E1464del) - ATRX_000172 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Groningen
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