Variant #0000326907 (NC_000002.11:g.27324340_27324390del, NM_000221.2:c.*1722_*1772del (KHK))

Chromosome 2
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.27324340_27324390del
DNA change (hg38) g.27101472_27101522del
Published as CGREF1(NM_001166239.1):c.795_845del (p.(Glu266_Ala282del))
ISCN -
DB-ID CGREF1_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
KHK NM_000221.2 -?/. - c.*1722_*1772del r.(=) p.(=)
CGREF1 NM_006569.5 -?/. - c.795_845del r.(?) p.(Glu266_Ala282del)


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