Variant #0000858751 (NC_000003.11:g.111312849C>T, NC_000003.11(NM_005816.4):c.808-4118C>T (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.111312849C>T
DNA change (hg38) -
Published as CD96(NM_198196.3):c.856-4118C>T
ISCN -
DB-ID CD96_000012
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) 9.0E-5 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 2022-05-09 15:51:19 +02:00 (CEST)
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.808-4118C>T r.(=) p.(=)
ZBED2 NM_024508.4 -?/. - c.200G>A r.(?) p.(Arg67His)


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