Variant #0000011743 (NC_000014.9:g.45176611G>T, FANCM(NM_020937.4):c.3857G>T)

Chromosome 14
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg38 / GRCh38) g.45176611G>T
Reference -
DB-ID FANCM_000053 See all 4 reported entries
dbSNP ID rs1888719897
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Guillermo Alberto-Instituto Fleming
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Protein     

Zygosity     

Co_ocurrence     

RNA change     

Review status     
FANCM NM_020937.4 ?/? 14 c.3857G>T p.(Ser1286Ile) Hetero no r.(?) -