Variant #0000690964 (NC_000011.9:g.119215111G>T, NC_000011.9(NM_031433.3):c.899-10C>A (MFRP))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.119215111G>T
DNA change (hg38) -
Published as C1QTNF5(NM_015645.4):c.-1738-10C>A, MFRP(NM_031433.3):c.899-10C>A
ISCN -
DB-ID C1QTNF5_000046
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
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.-3750C>A r.(?) p.(=)
C1QTNF5 NM_015645.3 -?/. - c.-1738-10C>A r.(=) p.(=)
MFRP NM_031433.3 -?/. - c.899-10C>A r.(=) p.(=)


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