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.

5 entries on 1 page. Showing entries 1 - 5.
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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     

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VIP     

Data_av     

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Panel size     

Owner     
+/+ 44i_46i c.(6237+1_6238-1)_(6354+1_6355-1)del r.(?) p.(?) FERM 2 (1902-2205) Parent #2 - pathogenic g.(76922383_76922865)_(76922983_76923996)del g.(77211338_77211820)_(77211938_77212951)del - - MYO7A_000559 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S, PCRq - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/+ 44i_46i c.(6237+1_6238-1)_(6354+1_6355-1)del r.(?) p.(?) FERM 2 (1902-2205) Parent #1 - pathogenic g.(76922383_76922865)_(76922983_76923996)del g.(77211338_77211820)_(77211938_77212951)del - - MYO7A_000559 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S, PCRq - - USH1B ? PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+/+ 44i_46i c.(6237+1_6238-1)_(6354+1_6355-1)del r.(?) p.(?) FERM 2 (1902-2205) Parent #1 - pathogenic g.(76922383_76922865)_(76922983_76923996)del g.(77211338_77211820)_(77211938_77212951)del - - MYO7A_000559 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S, PCRq - - USH1B ? PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
+/+ 44i_46i c.(6237+1_6238-1)_(6354+1_6355-1)del r.(?) p.(?) FERM 2 (1902-2205) Parent #1 - pathogenic g.(76922383_76922865)_(76922983_76923996)del g.(77211338_77211820)_(77211938_77212951)del - - MYO7A_000559 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S, PCRq - - USH1B ? PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+?/. 44i_46i c.(6237+1_6238-1)_(6354+1_6355-1)del r.spl? p.? - Parent #2 - likely pathogenic (recessive) g.(76922383_76922865)_(76922983_76923996)del g.(77211338_77211820)_(77211938_77212951)del - - MYO7A_000559 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC06471 PubMed: Khateb 2020 one affected brother F - - French - - - - 1 LOVD
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