Variant #0000292887 (NC_000004.11:g.120057719G>A, NM_016599.4:c.39G>A (MYOZ2))

Chromosome 4
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.120057719G>A
DNA change (hg38) g.119136564G>A
Published as MYOZ2(NM_016599.4):c.39G>A (p.Q13=, p.=), MYOZ2(NM_016599.5):c.39G>A (p.Q13=)
ISCN -
DB-ID MYOZ2_000038 See all 3 reported entries
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) 9.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYOZ2 NM_016599.4 -/. - c.39G>A r.(?) p.(Gln13=)


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