Variant #0000272895 (NC_000022.10:g.37964408_37964428del, NM_152243.2:c.757_777del (CDC42EP1))

Chromosome 22
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.37964408_37964428del
DNA change (hg38) g.37568401_37568421del
Published as CDC42EP1(NM_152243.3):c.757_777delCCAGCGCCTGCTGCAAACCCC (p.P253_P259del)
ISCN -
DB-ID CDC42EP1_000003
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
LGALS2 NM_006498.2 -/. - c.*1853_*1873del r.(=) p.(=)
CDC42EP1 NM_152243.2 -/. - c.757_777del r.(?) p.(Pro253_Pro259del)


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