Variant #0000979403 (NC_000011.9:g.119212576G>A, NM_001278431.1:c.-1215C>T (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.119212576G>A
DNA change (hg38) -
Published as MFRP(NM_031433.4):c.1506C>T (p.(Ser502=))
ISCN -
DB-ID RNF26_000010
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C1QTNF5 NM_001278431.1 ?/. - c.-1215C>T r.(?) p.(=)
RNF26 NM_032015.4 ?/. - c.*5442G>A r.(=) p.(=)


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