Variant #0000928969 (NC_000005.9:g.112102960C>T, NM_000038.5:c.295C>T (APC))

Chromosome 5
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.112102960C>T
DNA change (hg38) -
Published as APC(NM_000038.5):c.295C>T (p.(Arg99Trp)), APC(NM_000038.6):c.295C>T (p.R99W), APC(NM_001127511.1):c.295C>T (p.R99W), APC(NM_001127511.3):c.325C>T ...
ISCN -
DB-ID APC_000420 See all 12 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) 0.0004 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 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

Exon_old     

DNA change (cDNA)     

RNA change     

Protein     

Predicted     

Type/DNA     
APC NM_000038.5 ?/. - - c.295C>T r.(?) p.(Arg99Trp) - -


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