chr14-45175794-G-T
Variant summary
Our verdict is Benign. Variant got -20 ACMG points: 0P and 20B. BP4_StrongBP6_Very_StrongBS1BS2
The NM_020937.4(FANCM):c.3040G>T(p.Gly1014Cys) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00072 in 1,613,592 control chromosomes in the GnomAD database, including 9 homozygotes. In-silico tool predicts a benign outcome for this variant. 14/20 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★★).
Frequency
Consequence
NM_020937.4 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Benign. Variant got -20 ACMG points.
Transcripts
RefSeq
Ensembl
Frequencies
GnomAD3 genomes AF: 0.00369 AC: 561AN: 151982Hom.: 5 Cov.: 32
GnomAD3 exomes AF: 0.00106 AC: 266AN: 250010Hom.: 2 AF XY: 0.000739 AC XY: 100AN XY: 135296
GnomAD4 exome AF: 0.000408 AC: 597AN: 1461492Hom.: 4 Cov.: 32 AF XY: 0.000320 AC XY: 233AN XY: 727070
GnomAD4 genome AF: 0.00371 AC: 565AN: 152100Hom.: 5 Cov.: 32 AF XY: 0.00366 AC XY: 272AN XY: 74340
ClinVar
Submissions by phenotype
not specified Benign:2
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Fanconi anemia Benign:1
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not provided Benign:1
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FANCM-related disorder Benign:1
This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). -
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at