Variant #0000891789 (NC_000014.8:g.45605327A>G, NM_020937.2:c.93A>G (FANCM))

Chromosome 14
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.45605327A>G
DNA change (hg38) -
Published as FANCM(NM_020937.2):c.93A>G (p.R31=), FANCM(NM_020937.4):c.93A>G (p.R31=)
ISCN -
DB-ID FANCM_000065 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) 2.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +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     
FKBP3 NM_002013.3 -?/. - c.-1668T>C r.(?) p.(=) -
PRPF39 NM_017922.3 -?/. - c.*21211A>G r.(=) p.(=) -
FANCM NM_020937.2 -?/. - c.93A>G r.(?) p.(Arg31=) -


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