Variant #0000542696 (NC_000011.9:g.119216121G>A, NC_000011.9(NM_031433.2):c.641+9C>T (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.119216121G>A
DNA change (hg38) g.119345411G>A
Published as C1QTNF5(NM_015645.4):c.-1996+9C>T, C1QTNF5(NM_015645.5):c.-1996+9C>T, MFRP(NM_031433.3):c.641+9C>T, MFRP(NM_031433.4):c.641+9C>T
ISCN -
DB-ID C1QTNF5_000016 See all 2 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) 0.0039 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 2019-07-18 18:22:55 +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.-4760C>T r.(?) p.(=)
C1QTNF5 NM_015645.3 -/. - c.-1996+9C>T r.(=) p.(=)
MFRP NM_031433.2 -/. - c.641+9C>T r.(=) p.(=)


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