Variant #0000553522 (NC_000015.9:g.100273607_100273613dup, NM_152449.2:c.-243_-237dup (LYSMD4))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.100273607_100273613dup
DNA change (hg38) g.99733402_99733408dup
Published as LYSMD4(NM_001284420.1):c.53_59dupGGTCGCG (p.G23Sfs*13)
ISCN -
DB-ID LYSMD4_000001
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 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     
LYSMD4 NM_152449.2 +?/. - c.-243_-237dup r.(?) p.(=)


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