Variant #0000266577 (NC_000003.11:g.111356083G>C, NM_005816.4:c.1362G>C (CD96))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.111356083G>C
DNA change (hg38) g.111637236G>C
Published as CD96(NM_198196.3):c.1410G>C (p.P470=)
ISCN -
DB-ID CD96_000004 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) 0.99913 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CD96 NM_005816.4 -/. - c.1362G>C r.(?) p.(Pro454=)
ZBED2 NM_024508.4 -/. - c.-42802C>G r.(?) p.(=)


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