Variant #0000862637 (NC_000011.9:g.65655566G>C, NM_198897.1:c.123C>G (FIBP))

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.65655566G>C
DNA change (hg38) -
Published as FIBP(NM_004214.4):c.123C>G (p.(Ile41Met))
ISCN -
DB-ID CCDC85B_000003
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) 0.00035 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTSW NM_001335.3 -?/. - c.*4477G>C r.(=) p.(=)
FOSL1 NM_005438.3 -?/. - c.*4791C>G r.(=) p.(=)
CCDC85B NM_006848.2 -?/. - c.-2689G>C r.(?) p.(=)
FIBP NM_198897.1 -?/. - c.123C>G r.(?) p.(Ile41Met)


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