Full data view for gene CHM


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_000390.2 transcript reference sequence.

7 entries on 1 page. Showing entries 1 - 7.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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Owner     
-/- 4 c.265A>T r.(?) p.(Ser89Cys) - Parent #1 - benign g.85233820T>A g.85978816T>A 295C>T - CHM_000003 hemizygous; recurrent, found 5 times PubMed: Tarpey 2009; USMA-missense variant in MSV3d - rs145707160 Germline - - +HpyCH4V;-DdeI; - - DNA SEQ - - MRX;IDX 19377474-Pat? PubMed: Tarpey 2009 - ? - - - - - for details contact Lucy Raymond (flr24 @ cam.ac.uk) - 5 Lucy Raymond
-/- 4 c.265A>T r.(?) p.(Ser89Cys) - Parent #1 - benign g.85233820T>A g.85978816T>A 295C>T - CHM_000003 hemizygous PubMed: Neveling 2012; USMA-missense variant in MSV3d - rs145707160 Germline - - +HpyCH4V;-DdeI; - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Neveling 2012 Proband M - - - - - - - 1 Anne-Françoise Roux
-/- 4 c.265A>T r.(?) p.(Ser89Cys) - Unknown - benign g.85233820T>A g.85978816T>A 295C>T - CHM_000003 hemizygous PubMed: Neveling 2012; USMA-missense variant in MSV3d - rs145707160 Germline - - +HpyCH4V;-DdeI; - - DNA SEQ, SEQ-NG-S - - XLRP - PubMed: Neveling 2012 Proband M - - - - - - - 1 Anne-Françoise Roux
-/- 4 c.265A>T r.(?) p.(Ser89Cys) - Unknown - benign g.85233820T>A g.85978816T>A 295C>T - CHM_000003 hemizygous PubMed: Neveling 2012; USMA-missense variant in MSV3d - rs145707160 Germline - - +HpyCH4V;-DdeI; - - DNA SEQ, SEQ-NG-S - - XLRP - PubMed: Neveling 2012 Proband M - - - - - - - 1 Anne-Françoise Roux
-/- 4 c.265A>T r.(?) p.(Ser89Cys) - Maternal (confirmed) - benign g.85233820T>A g.85978816T>A 295C>T - CHM_000003 hemizygous PubMed: Neveling 2012; USMA-missense variant in MSV3d - rs145707160 Germline - - +HpyCH4V;-DdeI; - - DNA SEQ, SEQ-NG-S - - XLRP - PubMed: Neveling 2012 Proband M - - - - - - - 1 Anne-Françoise Roux
-/- 4 c.265A>T r.(?) p.(Ser89Cys) - Parent #1 - benign g.85233820T>A g.85978816T>A 295C>T - CHM_000003 heterozygous PubMed: Neveling 2012; USMA-missense variant in MSV3d - rs145707160 Germline - - +HpyCH4V;-DdeI; - - DNA SEQ, SEQ-NG-S - - XLRP - PubMed: Neveling 2012 Proband F - - - - - - - 1 Anne-Françoise Roux
-/- 4 c.265A>T r.(?) p.(Ser89Cys) - Maternal (inferred) - benign g.85233820T>A g.85978816T>A 295C>T - CHM_000003 hemizygous PubMed: Neveling 2012; USMA-missense variant in MSV3d - rs145707160 Germline - - +HpyCH4V;-DdeI; - - DNA SEQ, SEQ-NG-S - - XLRP - PubMed: Neveling 2012 Proband M - - - - - - - 1 Anne-Françoise Roux
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