Variant #0000246996 (NC_000011.9:g.119217067A>G, NM_031433.2:c.72T>C (MFRP))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.119217067A>G
DNA change (hg38) g.119346357A>G
Published as C1QTNF5(NM_015645.5):c.-2565T>C, MFRP(NM_031433.4):c.72T>C (p.P24=)
ISCN -
DB-ID C1QTNF5_000025
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) 0.00077 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C1QTNF5 NM_001278431.1 -/. - c.-5706T>C r.(?) p.(=)
C1QTNF5 NM_015645.3 -/. - c.-2565T>C r.(?) p.(=)
MFRP NM_031433.2 -/. - c.72T>C r.(?) p.(Pro24=)


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