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.

11 entries on 1 page. Showing entries 1 - 11.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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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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Disease     

ID_report     

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Owner     
+/+ 7 c.634C>T r.(?) p.(Arg212Cys) Motor domain (1-729) Unknown - pathogenic g.76867949C>T g.77156903C>T - - MYO7A_000002 Heterozygous PubMed: Weston 1996; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121965080 Germline - 0/192 controls - - - DNA SEQ - - USH1B ? PubMed: Weston 1996 Proband - - Belgium - - - - - 1 William J. Kimberling
+/+ 7 c.634C>T r.(?) p.(Arg212Cys) Motor domain (1-729) Unknown - pathogenic g.76867949C>T g.77156903C>T - - MYO7A_000002 Heterozygous PubMed: Weston 1996; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121965080 Germline - 0/192 controls - - - DNA SEQ - - USH1B ? PubMed: Weston 1996 Proband - - Netherlands - - - - - 1 William J. Kimberling
+/+ 7 c.634C>T r.(?) p.(Arg212Cys) Motor domain (1-729) Parent #1 - pathogenic g.76867949C>T g.77156903C>T - - MYO7A_000002 Heterozygous PubMed: Weston 1996; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121965080 Germline - 0/192 controls - - - DNA SEQ - - USH1B ? PubMed: Weston 1996 Proband - - Netherlands - - - - - 1 William J. Kimberling
+/+ 7 c.634C>T r.(?) p.(Arg212Cys) Motor domain (1-729) Parent #2 - pathogenic g.76867949C>T g.77156903C>T - - MYO7A_000002 Heterozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121965080 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 7 c.634C>T r.(?) p.(Arg212Cys) Motor domain (1-729) Parent #2 - pathogenic g.76867949C>T g.77156903C>T - - MYO7A_000002 Heterozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121965080 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Relative - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 7 c.634C>T r.(?) p.(Arg212Cys) Motor domain (1-729) Parent #2 - pathogenic g.76867949C>T g.77156903C>T - - MYO7A_000002 Heterozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121965080 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Relative - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 7 c.634C>T r.(?) p.(Arg212Cys) Motor domain (1-729) Unknown - pathogenic g.76867949C>T g.77156903C>T - - MYO7A_000002 Heterozygous PubMed: Weston 1996; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121965080 Germline - 0/192 controls - - - DNA SEQ - - USH1B ? PubMed: Weston 1996 Proband - - United States - - - - - 1 William J. Kimberling
+/+ 7 c.634C>T r.(?) p.(Arg212Cys) Motor domain (1-729) Unknown - pathogenic g.76867949C>T g.77156903C>T - - MYO7A_000002 Heterozygous PubMed: Weston 1996; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121965080 Germline - 0/192 controls - - - DNA SEQ - - USH1B ? PubMed: Weston 1996 Proband - - United States - - - - - 1 William J. Kimberling
+?/. - c.634C>T r.(?) p.(Arg212Cys) - Unknown - likely pathogenic g.76867949C>T g.77156903C>T - - MYO7A_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 7 c.634C>T r.(?) p.(Arg212Cys) - Both (homozygous) - pathogenic (recessive) g.76867949C>T g.77156903C>T - - MYO7A_000002 - PubMed: Cremers 2007 - - Germline - - - - - DNA PE - - retinal disease USH1-23 PubMed: Cremers 2007 - F no Denmark - - - - - 1 LOVD
+?/. - c.634C>T r.(?) p.(Arg212Cys) - Parent #1 - likely pathogenic g.76867949C>T g.77156903C>T MYO7A c.634C>T, p.R212C - MYO7A_000002 compound heterozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 138 PubMed: Jauregui 2020 - M - (United States) Hispanic - - - - 1 LOVD
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