Full data view for gene TMC1


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_138691.2 transcript reference sequence.

18 entries on 1 page. Showing entries 1 - 18.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

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Methylation     

Template     

Technique     

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Disease     

ID_report     

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Owner     
+/. 15 c.1165C>T r.(?) p.(Arg389*) - Maternal (confirmed) - pathogenic g.75404174C>T g.72789258C>T - - TMC1_000005 - PubMed: Brownstein 2011, Journal: Brownstein 2011 - - Germline yes 3/168 cases (het) - - - DNA SEQ-NG-I blood - DFNB7 - PubMed: Brownstein 2011, Journal: Brownstein 2011 2-generation family, 3 affected sibs (2F, M), unaffected heterozygous carrier parents/sibs F;M no Israel Morocco;Jewish - - - - 3 Zippi Brownstein
+/+ 15 c.1165C>T r.(?) p.(Arg389*) Extracellular 2 (387-440) Maternal (confirmed) - pathogenic g.75404174C>T g.72789258C>T in exon 13 - TMC1_000005 heterozygous; Pathogenic PubMed: Meyer 2004 - rs151001642 Germline - 0/584 controls none - - DNA SEQ - - DFNB - PubMed: Meyer 2004 Proband M - Sudan - - - - - 1 Anne-Françoise Roux
+/+ 15 c.1165C>T r.(?) p.(Arg389*) Extracellular 2 (387-440) Maternal (confirmed) - pathogenic g.75404174C>T g.72789258C>T in exon 13 - TMC1_000005 heterozygous; Pathogenic PubMed: Meyer 2004 - rs151001642 Germline - 0/584 controls none - - DNA SEQ - - DFNB - PubMed: Meyer 2004 Relative F - Sudan - - - - - 1 Anne-Françoise Roux
+/+ 15 c.1165C>T r.(?) p.(Arg389*) Extracellular 2 (387-440) Maternal (confirmed) - pathogenic g.75404174C>T g.72789258C>T in exon 13 - TMC1_000005 heterozygous; Pathogenic PubMed: Meyer 2004 - rs151001642 Germline - 0/584 controls none - - DNA SEQ - - DFNB - PubMed: Meyer 2004 Relative M - Sudan - - - - - 1 Anne-Françoise Roux
+/+ 15 c.1165C>T r.(?) p.(Arg389*) Extracellular 2 (387-440) Maternal (confirmed) - pathogenic g.75404174C>T g.72789258C>T in exon 13 - TMC1_000005 heterozygous; Pathogenic PubMed: Meyer 2004 - rs151001642 Germline - 0/584 controls none - - DNA SEQ - - DFNB - PubMed: Meyer 2004 Relative F - Sudan - - - - - 1 Anne-Françoise Roux
+/+ 15 c.1165C>T r.(?) p.(Arg389*) Extracellular 2 (387-440) Paternal (inferred) - pathogenic g.75404174C>T g.72789258C>T - - TMC1_000005 homozygous; Pathogenic PubMed: Tlili 2008 - rs151001642 Germline - 0/200 controls none - - DNA SEQ - - DFNB - PubMed: Tlili 2008 Proband F - Tunisia - - - - - 1 Anne-Françoise Roux
+/+ 15 c.1165C>T r.(?) p.(Arg389*) Extracellular 2 (387-440) Maternal (inferred) - pathogenic g.75404174C>T g.72789258C>T - - TMC1_000005 homozygous; Pathogenic PubMed: Tlili 2008 - rs151001642 Germline - 0/200 controls none - - DNA SEQ - - DFNB - PubMed: Tlili 2008 Proband F - Tunisia - - - - - 1 Anne-Françoise Roux
+/+ 15 c.1165C>T r.(?) p.(Arg389*) Extracellular 2 (387-440) Paternal (inferred) - pathogenic g.75404174C>T g.72789258C>T - - TMC1_000005 homozygous; Pathogenic PubMed: Hilgert 2008 - rs151001642 Germline - - none - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Proband F - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 15 c.1165C>T r.(?) p.(Arg389*) Extracellular 2 (387-440) Paternal (inferred) - pathogenic g.75404174C>T g.72789258C>T - - TMC1_000005 homozygous; Pathogenic PubMed: Hilgert 2008 - rs151001642 Germline - - none - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative F - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 15 c.1165C>T r.(?) p.(Arg389*) Extracellular 2 (387-440) Paternal (inferred) - pathogenic g.75404174C>T g.72789258C>T - - TMC1_000005 homozygous; Pathogenic PubMed: Hilgert 2008 - rs151001642 Germline - - none - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative M - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 15 c.1165C>T r.(?) p.(Arg389*) Extracellular 2 (387-440) Maternal (inferred) - pathogenic g.75404174C>T g.72789258C>T - - TMC1_000005 homozygous; Pathogenic PubMed: Hilgert 2008 - rs151001642 Germline - - none - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Proband F - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 15 c.1165C>T r.(?) p.(Arg389*) Extracellular 2 (387-440) Maternal (inferred) - pathogenic g.75404174C>T g.72789258C>T - - TMC1_000005 homozygous; Pathogenic PubMed: Hilgert 2008 - rs151001642 Germline - - none - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative F - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 15 c.1165C>T r.(?) p.(Arg389*) Extracellular 2 (387-440) Maternal (inferred) - pathogenic g.75404174C>T g.72789258C>T - - TMC1_000005 homozygous; Pathogenic PubMed: Hilgert 2008 - rs151001642 Germline - - none - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative M - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 15 c.1165C>T r.(?) p.(Arg389*) Extracellular 2 (387-440) Maternal (confirmed) - pathogenic g.75404174C>T g.72789258C>T - - TMC1_000005 heterozygous; Pathogenic PubMed: Brownstein 2011 - rs151001642 Germline - 0/164 controls none - - DNA SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Proband F - Morocco - - - - - 1 Anne-Françoise Roux
+/+ 15 c.1165C>T r.(?) p.(Arg389*) Extracellular 2 (387-440) Paternal (inferred) ACMG VUS g.75404174C>T g.72789258C>T - - TMC1_000005 homozygous PubMed: Besnard, Garcia-Garcia 2014 - rs151001642 Germline - - none - - DNA SEQ, SEQ-NG-S - - DFN - PubMed: Besnard, Garcia-Garcia 2014 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 15 c.1165C>T r.(?) p.(Arg389*) Extracellular 2 (387-440) Maternal (inferred) ACMG VUS g.75404174C>T g.72789258C>T - - TMC1_000005 homozygous PubMed: Besnard, Garcia-Garcia 2014 - rs151001642 Germline - - none - - DNA SEQ, SEQ-NG-S - - DFN - PubMed: Besnard, Garcia-Garcia 2014 Proband M - - - - - - - 1 Anne-Françoise Roux
+/. - c.1165C>T r.(?) p.(Arg389*) - Unknown - pathogenic g.75404174C>T - - - TMC1_000005 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.1165C>T r.(?) p.(Arg389Ter) - Unknown - pathogenic g.75404174C>T - - - TMC1_000005 - - - rs151001642 Unknown - - - - - - - - - - - - - - - - - - - - - - -
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