Full data view for gene MYO7A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_000260.3 transcript reference sequence.

15 entries on 1 page. Showing entries 1 - 15.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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+/. 7 c.689C>T r.(?) p.(Ala230Val) - Maternal (confirmed) - pathogenic g.76868004C>T g.77156958C>T - - MYO7A_000143 0/105 controls - - - Germline yes 2/148 patients - - - DNA SEQ-NG-I blood - DFNA11 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - no Israel Jewish-Ashkenazi - - - - 3 Zippi Brownstein
+/+ 7 c.689C>T r.(?) p.(Ala230Val) Motor domain (1-729) Unknown - pathogenic g.76868004C>T g.77156958C>T - - MYO7A_000143 Heterozygous PubMed: Di Leva 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls - - - DNA SEQ - - DFNA1 ? PubMed: Di Leva 2006 Proband F - Italy - - - - - 1 Anne-Françoise Roux
+/+ 7 c.689C>T r.(?) p.(Ala230Val) Motor domain (1-729) Parent #2 - pathogenic g.76868004C>T g.77156958C>T - - MYO7A_000143 Heterozygous PubMed: Di Leva 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls - - - DNA SEQ - - DFNA1 ? PubMed: Di Leva 2006 Relative M - Italy - - - - - 1 Anne-Françoise Roux
+/+ 7 c.689C>T r.(?) p.(Ala230Val) Motor domain (1-729) Parent #2 - pathogenic g.76868004C>T g.77156958C>T - - MYO7A_000143 Heterozygous PubMed: Di Leva 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls - - - DNA SEQ - - DFNA1 ? PubMed: Di Leva 2006 Relative M - Italy - - - - - 1 Anne-Françoise Roux
+/+ 7 c.689C>T r.(?) p.(Ala230Val) Motor domain (1-729) Parent #1 - pathogenic g.76868004C>T g.77156958C>T - - MYO7A_000143 Heterozygous PubMed: Di Leva 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls - - - DNA SEQ - - DFNA1 ? PubMed: Di Leva 2006 Relative M - Italy - - - - - 1 Anne-Françoise Roux
+/+ 7 c.689C>T r.(?) p.(Ala230Val) Motor domain (1-729) Parent #1 - pathogenic g.76868004C>T g.77156958C>T - - MYO7A_000143 Heterozygous PubMed: Di Leva 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls - - - DNA SEQ - - DFNA1 ? PubMed: Di Leva 2006 Relative M - Italy - - - - - 1 Anne-Françoise Roux
+/+ 7 c.689C>T r.(?) p.(Ala230Val) Motor domain (1-729) Parent #1 - pathogenic g.76868004C>T g.77156958C>T - - MYO7A_000143 Heterozygous PubMed: Di Leva 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls - - - DNA SEQ - - DFNA1 ? PubMed: Di Leva 2006 Relative - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 7 c.689C>T r.(?) p.(Ala230Val) Motor domain (1-729) Parent #1 - pathogenic g.76868004C>T g.77156958C>T - - MYO7A_000143 Heterozygous PubMed: Di Leva 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls - - - DNA SEQ - - DFNA1 ? PubMed: Di Leva 2006 Relative M - Italy - - - - - 1 Anne-Françoise Roux
+/+ 7 c.689C>T r.(?) p.(Ala230Val) Motor domain (1-729) Parent #1 - pathogenic g.76868004C>T g.77156958C>T - - MYO7A_000143 Heterozygous PubMed: Di Leva 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls - - - DNA SEQ - - DFNA1 ? PubMed: Di Leva 2006 Relative M - Italy - - - - - 1 Anne-Françoise Roux
+/+ 7 c.689C>T r.(?) p.(Ala230Val) Motor domain (1-729) Parent #1 - pathogenic g.76868004C>T g.77156958C>T - - MYO7A_000143 Heterozygous PubMed: Di Leva 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls - - - DNA SEQ - - DFNA1 ? PubMed: Di Leva 2006 Relative F - Italy - - - - - 1 Anne-Françoise Roux
+/+ 7 c.689C>T r.(?) p.(Ala230Val) Motor domain (1-729) Parent #1 - pathogenic g.76868004C>T g.77156958C>T - - MYO7A_000143 Heterozygous PubMed: Di Leva 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls - - - DNA SEQ - - DFNA1 ? PubMed: Di Leva 2006 Relative M - Italy - - - - - 1 Anne-Françoise Roux
+/+ 7 c.689C>T r.(?) p.(Ala230Val) Motor domain (1-729) Parent #1 - pathogenic g.76868004C>T g.77156958C>T - - MYO7A_000143 Heterozygous PubMed: Di Leva 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls - - - DNA SEQ - - DFNA1 ? PubMed: Di Leva 2006 Relative F - Italy - - - - - 1 Anne-Françoise Roux
+/. - c.689C>T r.(?) p.(Ala230Val) - Unknown - pathogenic g.76868004C>T - - - MYO7A_000143 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.689C>T r,(?) p.(Ala230Val) - Parent #1 - pathogenic g.76868004C>T g.77156958C>T - - MYO7A_000143 combination of alleles not reported PubMed: Wu 2019 - - Germline - 1/1291 cases hearing loss - - - DNA SEQ, SEQ-NG - 213-gene panel HL - PubMed: Wu 2019 analysis 1291 cases hearing loss - - Taiwan - - - - - 1 Johan den Dunnen
+/. - c.689C>T r.(?) p.(Ala230Val) - Unknown - pathogenic g.76868004C>T g.77156958C>T - - MYO7A_000143 - PubMed: Redfield 2024 - - Germline/De novo (untested) - - - - - DNA SEQ, SEQ-NG - WES HL patient PubMed: Redfield 2024 - - - China - - - - - 1 Johan den Dunnen
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