Variant #0000967884 (NC_000015.9:g.64458294del, NM_000942.4:c.-3097del (PPIB))

Chromosome 15
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.64458294del
DNA change (hg38) -
Published as CSNK1G1(NM_022048.5):c.*5848delT
ISCN -
DB-ID CSNK1G1_000004 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPIB NM_000942.4 -?/. - c.-3097del r.(?) p.(=)
KIAA0101 NM_014736.4 -?/. - c.*199947del r.(?) p.(=)
CSNK1G1 NM_022048.3 -?/. - c.*5848del r.(?) p.(=)
SNX22 NM_024798.2 -?/. - c.*11587del r.(?) p.(=)


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