Variant #0000999037 (NC_000011.9:g.44956503G>A, NM_006034.3:c.502C>T (TP53I11))

Chromosome 11
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.44956503G>A
DNA change (hg38) -
Published as TP53I11(NM_006034.3):c.502C>T (p.(Arg168Cys))
ISCN -
DB-ID TP53I11_000001
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) 1.0E-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     
TP53I11 NM_006034.3 -?/. - c.502C>T r.(?) p.(Arg168Cys)
TSPAN18 NM_130783.4 -?/. - c.*5774G>A r.(=) p.(=)


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