Variant #0000273026 (NC_000009.11:g.123205981C>T, NM_018249.4:c.3065G>A (CDK5RAP2))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.123205981C>T
DNA change (hg38) g.120443703C>T
Published as CDK5RAP2(NM_018249.5):c.3065G>A (p.G1022E)
ISCN -
DB-ID CDK5RAP2_000029 See all 3 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) 0.02501 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 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDK5RAP2 NM_018249.4 -/. - c.3065G>A r.(?) p.(Gly1022Glu)


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