Variant #0001054161 (NC_000011.9:g.119215338_119215341delinsAGTG, NC_000011.9(NM_031433.2):c.898+1_898+4delinsCACT (MFRP))

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.119215338_119215341delinsAGTG
DNA change (hg38) -
Published as MFRP(NM_031433.4):c.898+1_898+4delinsCACT
ISCN -
DB-ID C1QTNF5_000095
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 2025-11-01 13:22:20 +01:00 (CET)
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.-3980_-3977delinsCACT r.(?) p.(=)
C1QTNF5 NM_015645.3 ?/. - c.-1739+1_-1739+4delinsCACT r.spl? p.?
MFRP NM_031433.2 ?/. - c.898+1_898+4delinsCACT r.spl? p.?


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