Variant #0000679973 (NC_000014.8:g.45605574G>T, NM_020937.2:c.340G>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.45605574G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID FANCM_000060
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 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FKBP3 NM_002013.3 +/. - c.-1915C>A r.(?) p.(=) -
PRPF39 NM_017922.3 +/. - c.*21458G>T r.(=) p.(=) -
FANCM NM_020937.2 +/. - c.340G>T r.(?) p.(Gly114Ter) -


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