Variant #0000350283 (NC_000011.9:g.119216504C>T, NM_031433.2:c.406G>A (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.119216504C>T
DNA change (hg38) g.119345794C>T
Published as C1QTNF5(NM_015645.5):c.-2231G>A, MFRP(NM_031433.4):c.406G>A (p.V136M)
ISCN -
DB-ID C1QTNF5_000022 See all 4 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) 0.2656 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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.-5143G>A r.(?) p.(=)
C1QTNF5 NM_015645.3 -/. - c.-2231G>A r.(?) p.(=)
MFRP NM_031433.2 -/. - c.406G>A r.(?) p.(Val136Met)


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