Variant #0000993137 (NC_000003.11:g.111264208G>A, NM_005816.4:c.377G>A (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.111264208G>A
DNA change (hg38) -
Published as CD96(NM_005816.4):c.377G>A (p.(Gly126Asp))
ISCN -
DB-ID CD96_000020
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) 5.0E-5 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 2024-08-28 13:16:32 +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.377G>A r.(?) p.(Gly126Asp)
ZBED2 NM_024508.4 ?/. - c.*48184C>T r.(=) p.(=)


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