Variant #0000616723 (NC_000017.10:g.58236715C>T, NM_000717.3:c.869C>T (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.58236715C>T
DNA change (hg38) g.60159354C>T
Published as CA4(NM_000717.4):c.869C>T (p.P290L), CA4(NM_000717.5):c.869C>T (p.P290L)
ISCN -
DB-ID CA4_000002 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) 0.00096 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +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.869C>T r.(?) p.(Pro290Leu)
USP32 NM_032582.3 -?/. - c.*19901G>A r.(=) p.(=)


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