Variant #0000273566 (NC_000015.9:g.78403608G>A, NM_006383.3:c.97C>T (CIB2))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.78403608G>A
DNA change (hg38) g.78111266G>A
Published as CIB2(NM_006383.3):c.97C>T (p.R33*), CIB2(NM_006383.4):c.97C>T (p.R33*)
ISCN -
DB-ID CIB2_000006 See all 5 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) 6.0E-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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CIB2 NM_006383.3 +/. - c.97C>T r.(?) p.(Arg33Ter)


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