Variant #0000263905 (NC_000017.10:g.58227471G>C, NC_000017.10(NM_000717.3):c.58+18G>C (CA4))

Chromosome 17
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.58227471G>C
DNA change (hg38) g.60150110G>C
Published as CA4(NM_000717.5):c.58+18G>C
ISCN -
DB-ID CA4_000004
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) 0.00071 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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     
CA4 NM_000717.3 -?/. - c.58+18G>C r.(=) p.(=)
USP32 NM_032582.3 -?/. - c.*29145C>G r.(=) p.(=)


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