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.

21 entries on 1 page. Showing entries 1 - 21.
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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)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. - c.635G>A r.(?) p.(Arg212His) - Unknown - pathogenic g.76867950G>A g.77156904G>A MYO7A(NM_000260.3):c.635G>A (p.R212H), MYO7A(NM_000260.4):c.635G>A (p.(Arg212His)) - MYO7A_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/+ 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Paternal (confirmed) - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Heterozygous PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs28934610 Germline - 0/878 controls -BceAI - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Paternal (confirmed) - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Heterozygous PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs28934610 Germline - 0/878 controls -BceAI - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Paternal (inferred) - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Homozygous PubMed: Weston 1996; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs28934610 Germline - 0/192 controls -BceAI - - DNA SEQ - - USH1B ? PubMed: Weston 1996 Proband - - Belgium - - - - - 1 William J. Kimberling
+/+ 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Maternal (inferred) - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Homozygous PubMed: Weston 1996; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs28934610 Germline - 0/192 controls -BceAI - - DNA SEQ - - USH1B ? PubMed: Weston 1996 Proband - - Belgium - - - - - 1 William J. Kimberling
+/+ 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Paternal (inferred) - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Homozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs28934610 Germline - - -BceAI - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Proband - - Belgium - - - - - 1 Anne-Françoise Roux
+/+ 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Maternal (inferred) - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Homozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs28934610 Germline - - -BceAI - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Proband - - Belgium - - - - - 1 Anne-Françoise Roux
+/+ 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Paternal (inferred) - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Homozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs28934610 Germline - - -BceAI - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Proband - - Belgium - - - - - 1 Anne-Françoise Roux
+/+ 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Maternal (inferred) - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Homozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs28934610 Germline - - -BceAI - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Proband - - Belgium - - - - - 1 Anne-Françoise Roux
+/+ 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Parent #2 - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Heterozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs28934610 Germline - - -BceAI - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Parent #2 - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Heterozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs28934610 Germline - - -BceAI - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Relative - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Parent #1 - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Heterozygous PubMed: Weston 1996; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs28934610 Germline - 0/192 controls -BceAI - - DNA SEQ - - USH1B ? PubMed: Weston 1996 Proband - - United States - - - - - 1 William J. Kimberling
+/+ 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Paternal (inferred) - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Homozygous Weston 1998 - rs28934610 Germline - 0/192 controls -BceAI - - DNA SEQ - - USH1B ? Weston 1998 Proband - - United States - - - - - 1 William J. Kimberling
+/+ 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Maternal (inferred) - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Homozygous Weston 1998 - rs28934610 Germline - 0/192 controls -BceAI - - DNA SEQ - - USH1B ? Weston 1998 Proband - - United States - - - - - 1 William J. Kimberling
+/+ 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Paternal (confirmed) - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs28934610 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+/+ 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Maternal (confirmed) - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs28934610 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+/+ 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Paternal (inferred) - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Homozygous PubMed: Abdi 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs28934610 Germline - 0/192 controls -BceAI - - DNA SEQ - - USH1B ? PubMed: Abdi 2016 Proband F - Algeria - - - - - 1 Crystel Bonnet
+/+ 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Maternal (inferred) - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Homozygous PubMed: Abdi 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs28934610 Germline - 0/192 controls -BceAI - - DNA SEQ - - USH1B ? PubMed: Abdi 2016 Proband F - Algeria - - - - - 1 Crystel Bonnet
+/? 7 c.635G>A r.(?) p.(Arg212His) Motor domain (1-729) Unknown - pathogenic g.76867950G>A g.77156904G>A - - MYO7A_000004 Heterozygous PubMed: Baux, Vaché 2017; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs28934610 Germline - - -BceAI - - DNA SEQ, SEQ-NG-S - - DFNB S1692 PubMed: Baux 2017 Proband F - France - - - - - 1 Anne-Françoise Roux
+/. - c.635G>A r.(?) p.(Arg212His) - Unknown - pathogenic g.76867950G>A - MYO7A(NM_000260.3):c.635G>A (p.R212H), MYO7A(NM_000260.4):c.635G>A (p.(Arg212His)) - MYO7A_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.635G>A r.(?) p.(Arg212His) - Unknown - pathogenic g.76867950G>A - MYO7A(NM_000260.3):c.635G>A (p.R212H), MYO7A(NM_000260.4):c.635G>A (p.(Arg212His)) - MYO7A_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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