Variant #0000724771 (NC_000014.8:g.45667921C>T, NM_020937.2:c.5791C>T (FANCM))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45667921C>T
DNA change (hg38) -
Published as FANCM(NM_020937.4):c.5791C>T (p.R1931*)
ISCN -
DB-ID FANCM_000004 See all 12 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) 0.00103 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
MIS18BP1 NM_018353.4 +/. - c.*5391G>A r.(=) p.(=) -
FANCM NM_020937.2 +/. - c.5791C>T r.(?) p.(Arg1931Ter) -


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