Variant #0000329542 (NC_000003.11:g.111342667A>T, NM_005816.4:c.1247A>T (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.111342667A>T
DNA change (hg38) g.111623820A>T
Published as CD96(NM_005816.4):c.1247A>T (p.(Gln416Leu))
ISCN -
DB-ID CD96_000003
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) 0.00041 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CD96 NM_005816.4 ?/. - c.1247A>T r.(?) p.(Gln416Leu)
ZBED2 NM_024508.4 ?/. - c.-29386T>A r.(?) p.(=)


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