Variant #0000522712 (NC_000004.11:g.56847410_56847412del, NM_025009.4:c.1644_1646del (CEP135))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.56847410_56847412del
DNA change (hg38) g.55981244_55981246del
Published as CEP135(NM_025009.4):c.1643_1645del (p.(Ala549del)), CEP135(NM_025009.4):c.1644_1646delTGC (p.A549del)
ISCN -
DB-ID CEP135_000011 See all 2 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEP135 NM_025009.4 -?/. - c.1644_1646del r.(?) p.(Ala549del)


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