Variant #0000250175 (NC_000014.8:g.45605463A>G, NM_020937.2:c.229A>G (FANCM))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.45605463A>G
DNA change (hg38) g.45136260A>G
Published as FANCM(NM_001308133.1):c.229A>G (p.(Thr77Ala)), FANCM(NM_020937.4):c.229A>G (p.T77A)
ISCN -
DB-ID FANCM_000008 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) 0.01142 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +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.-1804T>C r.(?) p.(=) -
PRPF39 NM_017922.3 -/. - c.*21347A>G r.(=) p.(=) -
FANCM NM_020937.2 -/. - c.229A>G r.(?) p.(Thr77Ala) -


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