NM_001204526.1:c.-26A>C
Variant summary
Our verdict is Benign. Variant got -8 ACMG points: 0P and 8B. BP4_ModerateBP6_ModerateBS2
The NM_001204526.1(SSR4):c.-26A>C variant causes a 5 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000503 in 1,168,137 control chromosomes in the GnomAD database, including 6 homozygotes. There are 147 hemizygotes in GnomAD. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).
Frequency
Consequence
NM_001204526.1 5_prime_UTR
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Benign. Variant got -8 ACMG points.
Transcripts
RefSeq
Ensembl
Frequencies
GnomAD3 genomes AF: 0.00295 AC: 334AN: 113298Hom.: 3 Cov.: 26 AF XY: 0.00271 AC XY: 96AN XY: 35448
GnomAD3 exomes AF: 0.000686 AC: 79AN: 115236Hom.: 0 AF XY: 0.000300 AC XY: 12AN XY: 40020
GnomAD4 exome AF: 0.000243 AC: 256AN: 1054786Hom.: 3 Cov.: 31 AF XY: 0.000148 AC XY: 51AN XY: 344392
GnomAD4 genome AF: 0.00293 AC: 332AN: 113351Hom.: 3 Cov.: 26 AF XY: 0.00270 AC XY: 96AN XY: 35511
ClinVar
Submissions by phenotype
not specified Benign:1
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. -
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at