Full data view for gene MYO15A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_016239.3 transcript reference sequence.

6 entries on 1 page. Showing entries 1 - 6.
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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     

VIP     

Methylation     

Template     

Technique     

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Disease     

ID_report     

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Panel size     

Owner     
+/+ 2 c.1185dup r.(?) p.(Glu396Argfs*36) N-terminal domain (1-1223) Both (homozygous) - pathogenic (recessive) g.18023299dup g.18119985dup 1185dupC - MYO15A_000030 - PubMed: Bashir et al., 2012 - - Germline yes - none - - DNA SEQ - - DFNB HLRB3 PubMed: Bashir 2012, PubMed: Naz 2017 family, 3 affected F - Pakistan - - - - - 3 Anne-Françoise Roux
+/+ 2 c.1185dup r.(?) p.(Glu396Argfs*36) N-terminal domain (1-1223) Paternal (confirmed) - pathogenic g.18023299dup g.18119985dup 1179_1185insC - MYO15A_000030 Heterozygous PubMed: Miyagawa et al., 2013 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Miyagawa et al., 2013 proband M - Japan - - - - - 1 Anne-Françoise Roux
+/+ 2 c.1185dup r.(?) p.(Glu396Argfs*36) N-terminal domain (1-1223) Paternal (confirmed) - pathogenic g.18023299dup g.18119985dup 1179_1185insC - MYO15A_000030 Heterozygous PubMed: Miyagawa et al., 2013 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Miyagawa et al., 2013 relative M - Japan - - - - - 1 Anne-Françoise Roux
?/. - c.1185dup r.(?) p.(Glu396Argfs*36) - Unknown ACMG pathogenic (recessive) g.18023299dup g.18119985dup 1185dupC - MYO15A_000030 - PubMed: Kim 2022, Journal: Kim 2022 - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - DFNA1 - PubMed: Kim 2022, Journal: Kim 2022 - - - Korea, South (Republic) - - - - - 1 So Young Kim
+/. - c.1185dup r.(?) p.(Glu396ArgfsTer36) - Unknown ACMG pathogenic (recessive) g.18023299dup g.18119985dup - - MYO15A_000030 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? MISC-315 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - 1 Johan den Dunnen
?/. - c.1185dupC r.(?) p.(Glu396Argfs*36) - Unknown ACMG pathogenic (recessive) g.18023299dup g.18119985dup 1185dupC - MYO15A_000030 - PubMed: Kim 2022, Journal: Kim 2022 - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - DFNA1 - PubMed: Kim 2022, Journal: Kim 2022 - - - Korea, South (Republic) - - - - - 1 So Young Kim
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