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.

4 entries on 1 page. Showing entries 1 - 4.
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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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VIP     

Data_av     

Treatment     

Panel size     

Owner     
-?/? 31 c.6614C>T r.(?) p.(Thr2205Ile) MyTH4 1 (2065-2217) Both (homozygous) ACMG VUS g.18051447C>T g.18148133C>T - - MYO15A_000020 homozygous, {MSV3dQ9UKN7:p.Thr2205Ile} PubMed: Nal et al., 2007 - rs121908970 Germline - 2/294 controls +SfaNI - - DNA SEQ - - DFNB - PubMed: Nal et al., 2007 proband - - Pakistan - - - - - 1 Anne-Françoise Roux
+?/? 31 c.6614C>T r.(?) p.(Thr2205Ile) MyTH4 1 (2065-2217) Maternal (confirmed) ACMG VUS g.18051447C>T g.18148133C>T - - MYO15A_000020 hemizygous, {MSV3dQ9UKN7:p.Thr2205Ile} PubMed: Liburd et al., 2001 - rs121908970 Germline - 0/720 controls +SfaNI - - DNA SEQ - - SMS - PubMed: Liburd et al., 2001 proband - - - - - - - - 1 Anne-Françoise Roux
-?/. - c.6614C>T r.(?) p.(Thr2205Ile) - Parent #1 - likely benign g.18051447C>T g.18148133C>T - - MYO15A_000020 9 heterozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs121908970 Germline - 9/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 9 Mohammed Faruq
-?/. - c.6614C>T r.(?) p.(Thr2205Ile) - Both (homozygous) - likely benign g.18051447C>T g.18148133C>T - - MYO15A_000020 1 homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs121908970 Germline - 1/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 1 Mohammed Faruq
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