Variant #0000253541 (NC_000017.10:g.58234012A>G, NM_000717.3:c.204A>G (CA4))

Chromosome 17
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.58234012A>G
DNA change (hg38) g.60156651A>G
Published as CA4(NM_000717.4):c.204A>G (p.G68=)
ISCN -
DB-ID CA4_000006
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) 0.00341 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 2020-07-14 10:25:45 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CA4 NM_000717.3 -/. - c.204A>G r.(?) p.(Gly68=)
USP32 NM_032582.3 -/. - c.*22604T>C r.(=) p.(=)


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