Full data view for gene MYO6


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_004999.3 transcript reference sequence.

8 entries on 1 page. Showing entries 1 - 8.
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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     

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Template     

Technique     

Tissue     

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Disease     

ID_report     

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VIP     

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Owner     
+?/. 34 c.3610C>T r.(?) p.(Arg1204Trp) - Parent #1 - likely pathogenic g.76623950C>T g.75914233C>T - - MYO6_000017 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - Germline - - - - - DNA SEQ-NG - - deafness - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - 1 Mieke Wesdorp
+/. - c.3610C>T r.(?) p.(Arg1204Trp) - Unknown - pathogenic g.76623950C>T g.75914233C>T - - MYO6_000017 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/? 34 c.3610C>T r.(?) p.(Arg1204Trp) - Paternal (inferred) ACMG VUS g.76623950C>T g.75914233C>T - - MYO6_000017 heterozygous, {MSV3dQ9UM54:p.(Arg1204Trp)} PubMed: Oonk et al., 2013 - - Germline - 0/362 controls - - - DNA SEQ, SEQ-NG-S - - DFNA1 - PubMed: Oonk et al., 2013 proband F - Netherlands - - - - - 1 Anne-Françoise Roux
+?/? 34 c.3610C>T r.(?) p.(Arg1204Trp) - Maternal (inferred) ACMG VUS g.76623950C>T g.75914233C>T - - MYO6_000017 heterozygous, {MSV3dQ9UM54:p.(Arg1204Trp)} PubMed: Oonk et al., 2013 - - Germline - 0/362 controls - - - DNA SEQ - - DFNA1 - PubMed: Oonk et al., 2013 relative F - Netherlands - - - - - 1 Anne-Françoise Roux
+?/? 34 c.3610C>T r.(?) p.(Arg1204Trp) - Paternal (inferred) ACMG VUS g.76623950C>T g.75914233C>T - - MYO6_000017 heterozygous, {MSV3dQ9UM54:p.(Arg1204Trp)} PubMed: Oonk et al., 2013 - - Germline - 0/362 controls - - - DNA SEQ - - DFNA1 - PubMed: Oonk et al., 2013 relative F - Netherlands - - - - - 1 Anne-Françoise Roux
+?/? 34 c.3610C>T r.(?) p.(Arg1204Trp) - Paternal (inferred) ACMG VUS g.76623950C>T g.75914233C>T - - MYO6_000017 heterozygous, {MSV3dQ9UM54:p.(Arg1204Trp)} PubMed: Oonk et al., 2013 - - Germline - 0/362 controls - - - DNA SEQ - - DFNA1 - PubMed: Oonk et al., 2013 relative M - Netherlands - - - - - 1 Anne-Françoise Roux
+?/? 34 c.3610C>T r.(?) p.(Arg1204Trp) - Maternal (inferred) ACMG VUS g.76623950C>T g.75914233C>T - - MYO6_000017 heterozygous, {MSV3dQ9UM54:p.(Arg1204Trp)} PubMed: Oonk et al., 2013 - - Germline - 0/362 controls - - - DNA SEQ - - DFNA1 - PubMed: Oonk et al., 2013 relative F - Netherlands - - - - - 1 Anne-Françoise Roux
?/. - c.3610C>T r.(?) p.(Arg1204Trp) - Unknown - VUS g.76623950C>T g.75914233C>T - - MYO6_000017 ACMG PP1, PP3 PubMed: Kim 2022, Journal: Kim 2022 - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - HL SH314-710 PubMed: Kim 2022, Journal: Kim 2022 - - - Korea, South (Republic) - - - - - 1 So Young Kim
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