Variant #0000325930 (NC_000018.9:g.57122151C>T, NM_133459.3:c.586G>A (CCBE1))

Chromosome 18
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.57122151C>T
DNA change (hg38) g.59454919C>T
Published as CCBE1(NM_133459.3):c.586G>A (p.(Gly196Arg)), CCBE1(NM_133459.4):c.586G>A (p.G196R)
ISCN -
DB-ID CCBE1_000017 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) 9.0E-5 View details
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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCBE1 NM_133459.3 -?/. - c.586G>A r.(?) p.(Gly196Arg)


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