Variant #0001015003 (NC_000012.11:g.57431331_57431332inv, NC_000012.11(NM_005379.3):c.2055_2055+1inv (MYO1A))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.57431331_57431332inv
DNA change (hg38) -
Published as MYO1A(NM_001256041.1):c.2055_2055+1delTGinsCT
ISCN -
DB-ID MYO1A_000043
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYO1A NM_005379.3 +/. - c.2055_2055+1inv r.spl? p.?


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