Variant #0000949606 (NC_000011.9:g.119216975T>C, NC_000011.9(NM_031433.2):c.157+7A>G (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.119216975T>C
DNA change (hg38) -
Published as C1QTNF5(NM_015645.5):c.-2480+7A>G
ISCN -
DB-ID C1QTNF5_000093
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) 0.00017 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 2023-11-27 17:35:39 +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.-5614A>G r.(?) p.(=)
C1QTNF5 NM_015645.3 -?/. - c.-2480+7A>G r.(=) p.(=)
MFRP NM_031433.2 -?/. - c.157+7A>G r.(=) p.(=)


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