Variant #0000801974 (NC_000005.9:g.150036327_150036338del, NM_007286.5:c.2390_2401del (SYNPO))

Chromosome 5
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.150036327_150036338del
DNA change (hg38) -
Published as SYNPO(NM_007286.6):c.2390_2401delCCCCGCCCCCGC (p.P797_P800del)
ISCN -
DB-ID SYNPO_000002
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYOZ3 NM_001122853.2 -/. - c.-4664_-4653del r.(?) p.(=)
SYNPO NM_007286.5 -/. - c.2390_2401del r.(?) p.(Pro797_Pro800del)


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