Variant #0000548729 (NC_000012.11:g.57430539_57430540del, NC_000012.11(NM_005379.3):c.2274+20_2274+21del (MYO1A))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.57430539_57430540del
DNA change (hg38) g.57036755_57036756del
Published as MYO1A(NM_001256041.2):c.2274+20_2274+21delAG
ISCN -
DB-ID MYO1A_000017
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYO1A NM_005379.3 -/. - c.2274+20_2274+21del r.(=) p.(=)


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