Variant #0000980909 (NC_000014.8:g.45605503C>T, NM_020937.2:c.269C>T (FANCM))

Chromosome 14
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.45605503C>T
DNA change (hg38) -
Published as FANCM(NM_020937.4):c.269C>T (p.(Pro90Leu))
ISCN -
DB-ID FANCM_000120 See all 3 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) 0.00029 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 2024-04-19 20:27:30 +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     

Haplotype     
FKBP3 NM_002013.3 ?/. - c.-1844G>A r.(?) p.(=) -
PRPF39 NM_017922.3 ?/. - c.*21387C>T r.(=) p.(=) -
FANCM NM_020937.2 ?/. - c.269C>T r.(?) p.(Pro90Leu) -


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