Variant #0000566707 (NC_000019.9:g.19651230G>A, NM_153221.2:c.381G>A (CILP2))

Chromosome 19
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.19651230G>A
DNA change (hg38) g.19540421G>A
Published as CILP2(NM_153221.2):c.381G>A (p.E127=)
ISCN -
DB-ID CILP2_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 2020-07-15 16:32:35 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CILP2 NM_153221.2 -?/. - c.381G>A r.(?) p.(Glu127=)
YJEFN3 NM_198537.3 -?/. - c.*2897G>A r.(=) p.(=)


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