14-19920906-A-G
Variant summary
Our verdict is Likely benign. The variant received -5 ACMG points: 0P and 5B. BP4_StrongBP7
The NM_001005483.1(OR4K5):c.300A>G(p.Gln100Gln) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000075 in 1,614,158 control chromosomes in the GnomAD database, including 1 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.
Frequency
Consequence
NM_001005483.1 synonymous
Scores
Clinical Significance
Conservation
Publications
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ACMG classification
Our verdict: Likely_benign. The variant received -5 ACMG points.
Variant Effect in Transcripts
ACMG analysis was done for transcript: NM_001005483.1. You can select a different transcript below to see updated ACMG assignments.
Frequencies
GnomAD3 genomes AF: 0.0000723 AC: 11AN: 152194Hom.: 0 Cov.: 36 show subpopulations
GnomAD2 exomes AF: 0.0000557 AC: 14AN: 251286 AF XY: 0.0000368 show subpopulations
GnomAD4 exome AF: 0.0000752 AC: 110AN: 1461846Hom.: 1 Cov.: 32 AF XY: 0.0000784 AC XY: 57AN XY: 727224 show subpopulations
Age Distribution
GnomAD4 genome AF: 0.0000722 AC: 11AN: 152312Hom.: 0 Cov.: 36 AF XY: 0.000121 AC XY: 9AN XY: 74478 show subpopulations
Age Distribution
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at