Variant #0000266629 (NC_000009.11:g.21974760C>G, NM_000077.4:c.67G>C (CDKN2A))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.21974760C>G
DNA change (hg38) g.21974761C>G
Published as CDKN2A(NM_001195132.2):c.67G>C (p.G23R)
ISCN -
DB-ID CDKN2A_000011 See all 4 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDKN2A NM_000077.4 +?/. - c.67G>C r.(?) p.(Gly23Arg)
CDKN2A NM_058195.3 +?/. - c.194-3553G>C r.(=) p.(=)


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