Variant #0000676784 (NC_000003.11:g.111319710C>T, NM_005816.4:c.1036C>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.111319710C>T
DNA change (hg38) -
Published as CD96(NM_005816.5):c.1036C>T (p.(Pro346Ser)), CD96(NM_198196.2):c.1084C>T (p.P362S)
ISCN -
DB-ID CD96_000010 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) 0.00022 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CD96 NM_005816.4 ?/. - c.1036C>T r.(?) p.(Pro346Ser)
ZBED2 NM_024508.4 ?/. - c.-6429G>A r.(?) p.(=)


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