Variant #0000949605 (NC_000011.9:g.119210455G>T, NM_001278431.1:c.318C>A (C1QTNF5))

Chromosome 11
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.119210455G>T
DNA change (hg38) -
Published as C1QTNF5(NM_015645.5):c.318C>A (p.F106L)
ISCN -
DB-ID RNF26_000008
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C1QTNF5 NM_001278431.1 ?/. - c.318C>A r.(?) p.(Phe106Leu)
RNF26 NM_032015.4 ?/. - c.*3321G>T r.(=) p.(=)


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