chr2-17932347-C-T
Variant summary
Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2BP4_Moderate
The NM_002252.5(KCNS3):c.1339C>T(p.Arg447Trp) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0000787 in 1,614,030 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 Uncertain significance (★). Another variant affecting the same amino acid position, but resulting in a different missense (i.e. R447Q) has been classified as Uncertain significance.
Frequency
Consequence
NM_002252.5 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Uncertain_significance. Variant got 0 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
KCNS3 | NM_002252.5 | c.1339C>T | p.Arg447Trp | missense_variant | 3/3 | ENST00000304101.9 | |
KCNS3 | NM_001282428.2 | c.1339C>T | p.Arg447Trp | missense_variant | 3/3 | ||
KCNS3 | XM_011532825.2 | c.1339C>T | p.Arg447Trp | missense_variant | 4/4 | ||
KCNS3 | XM_047444255.1 | c.1339C>T | p.Arg447Trp | missense_variant | 3/3 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
KCNS3 | ENST00000304101.9 | c.1339C>T | p.Arg447Trp | missense_variant | 3/3 | 1 | NM_002252.5 | P1 | |
KCNS3 | ENST00000403915.5 | c.1339C>T | p.Arg447Trp | missense_variant | 3/3 | 1 | P1 | ||
KCNS3 | ENST00000465292.5 | n.305+14476C>T | intron_variant, non_coding_transcript_variant | 4 |
Frequencies
GnomAD3 genomes ? AF: 0.000138 AC: 21AN: 152148Hom.: 0 Cov.: 32
GnomAD3 exomes AF: 0.0000716 AC: 18AN: 251222Hom.: 0 AF XY: 0.000103 AC XY: 14AN XY: 135758
GnomAD4 exome AF: 0.0000725 AC: 106AN: 1461764Hom.: 0 Cov.: 41 AF XY: 0.0000784 AC XY: 57AN XY: 727166
GnomAD4 genome ? AF: 0.000138 AC: 21AN: 152266Hom.: 0 Cov.: 32 AF XY: 0.000188 AC XY: 14AN XY: 74452
ClinVar
Submissions by phenotype
not specified Uncertain:1
Uncertain significance, criteria provided, single submitter | clinical testing | Ambry Genetics | Jan 26, 2022 | The c.1339C>T (p.R447W) alteration is located in exon 3 (coding exon 1) of the KCNS3 gene. This alteration results from a C to T substitution at nucleotide position 1339, causing the arginine (R) at amino acid position 447 to be replaced by a tryptophan (W). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. - |
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at