chr11-3666424-G-A
Variant summary
Our verdict is Uncertain significance. Variant got 1 ACMG points: 2P and 1B. PM2BP4
The NM_020402.4(CHRNA10):c.1036C>T(p.Arg346Trp) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000127 in 1,613,840 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. 12/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).
Frequency
Consequence
NM_020402.4 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Uncertain_significance. Variant got 1 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
CHRNA10 | NM_020402.4 | c.1036C>T | p.Arg346Trp | missense_variant | 5/5 | ENST00000250699.2 | |
CHRNA10 | NM_001303034.2 | c.418C>T | p.Arg140Trp | missense_variant | 5/5 | ||
CHRNA10 | NM_001303035.2 | c.418C>T | p.Arg140Trp | missense_variant | 5/5 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
CHRNA10 | ENST00000250699.2 | c.1036C>T | p.Arg346Trp | missense_variant | 5/5 | 1 | NM_020402.4 | P1 | |
CHRNA10 | ENST00000534359.1 | c.*117C>T | 3_prime_UTR_variant | 5/5 | 1 | ||||
CHRNA10 | ENST00000526599.1 | c.*807C>T | 3_prime_UTR_variant, NMD_transcript_variant | 5/5 | 1 |
Frequencies
GnomAD3 genomes AF: 0.000131 AC: 20AN: 152222Hom.: 0 Cov.: 32
GnomAD3 exomes AF: 0.000116 AC: 29AN: 250812Hom.: 0 AF XY: 0.000118 AC XY: 16AN XY: 135562
GnomAD4 exome AF: 0.000127 AC: 185AN: 1461618Hom.: 0 Cov.: 31 AF XY: 0.000118 AC XY: 86AN XY: 727116
GnomAD4 genome AF: 0.000131 AC: 20AN: 152222Hom.: 0 Cov.: 32 AF XY: 0.0000941 AC XY: 7AN XY: 74366
ClinVar
Submissions by phenotype
not specified Uncertain:1
Uncertain significance, criteria provided, single submitter | clinical testing | Ambry Genetics | Oct 26, 2022 | The c.1036C>T (p.R346W) alteration is located in exon 5 (coding exon 5) of the CHRNA10 gene. This alteration results from a C to T substitution at nucleotide position 1036, causing the arginine (R) at amino acid position 346 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