Variant #0000800888 (NC_000003.11:g.111298048dup, NM_005816.4:c.718dup (CD96))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.111298048dup
DNA change (hg38) -
Published as CD96(NM_005816.5):c.718dup (p.(Ile240Asnfs*13)), CD96(NM_198196.2):c.766dupA (p.I256Nfs*13)
ISCN -
DB-ID CD96_000011 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CD96 NM_005816.4 ?/. - c.718dup r.(?) p.(Ile240Asnfs*13)
ZBED2 NM_024508.4 ?/. - c.*14347dup r.(?) p.(=)


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