Variant #0000979405 (NC_000011.9:g.119216279del, NM_031433.2:c.498del (MFRP))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.119216279del
DNA change (hg38) -
Published as MFRP(NM_031433.4):c.498del (p.(Asn167ThrfsTer25)), MFRP(NM_031433.4):c.498delC (p.N167Tfs*25)
ISCN -
DB-ID C1QTNF5_000020 See all 28 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) 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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C1QTNF5 NM_001278431.1 +/. - c.-4912del r.(?) p.(=)
C1QTNF5 NM_015645.3 +/. - c.-2139del r.(?) p.(=)
MFRP NM_031433.2 +/. - c.498del r.(?) p.(Asn167ThrfsTer25)


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