Variant #0001051439 (NC_000003.11:g.111297908A>C, NM_005816.4:c.578A>C (CD96))

Chromosome 3
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.111297908A>C
DNA change (hg38) -
Published as CD96(NM_005816.5):c.578A>C (p.(Gln193Pro))
ISCN -
DB-ID CD96_000030
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) 0.00135 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CD96 NM_005816.4 -?/. - c.578A>C r.(?) p.(Gln193Pro)
ZBED2 NM_024508.4 -?/. - c.*14484T>G r.(=) p.(=)


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