NM_003924.4:c.759G>A
Variant summary
Our verdict is Benign. Variant got -17 ACMG points: 0P and 17B. BP4_StrongBP6_Very_StrongBP7BS2
The NM_003924.4(PHOX2B):c.759G>A(p.Ala253Ala) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0000223 in 1,209,260 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★★).
Frequency
Consequence
NM_003924.4 synonymous
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Benign. Variant got -17 ACMG points.
Transcripts
RefSeq
Ensembl
Frequencies
GnomAD3 genomes AF: 0.0000341 AC: 5AN: 146714Hom.: 0 Cov.: 32
GnomAD3 exomes AF: 0.0000745 AC: 1AN: 13430Hom.: 0 AF XY: 0.00 AC XY: 0AN XY: 8164
GnomAD4 exome AF: 0.0000207 AC: 22AN: 1062546Hom.: 0 Cov.: 31 AF XY: 0.0000216 AC XY: 11AN XY: 508164
GnomAD4 genome AF: 0.0000341 AC: 5AN: 146714Hom.: 0 Cov.: 32 AF XY: 0.0000280 AC XY: 2AN XY: 71372
ClinVar
Submissions by phenotype
Hereditary cancer-predisposing syndrome Benign:2
This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. -
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Haddad syndrome Benign:1
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Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at