Variant #0000865394 (NC_000017.10:g.58234066C>T, NM_000717.3:c.258C>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.58234066C>T
DNA change (hg38) -
Published as CA4(NM_000717.4):c.258C>T (p.N86=), CA4(NM_000717.5):c.258C>T (p.N86=)
ISCN -
DB-ID CA4_000008 See all 2 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) 0.00036 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 2022-05-09 16:01:56 +02:00 (CEST)
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.258C>T r.(?) p.(Asn86=)
USP32 NM_032582.3 -?/. - c.*22550G>A r.(=) p.(=)


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