11-3666331-C-T
Variant summary
Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2BP4_Moderate
The NM_020402.4(CHRNA10):c.1129G>A(p.Gly377Ser) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000496 in 1,613,190 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. 16/21 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 0 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | Exon rank | MANE | Protein | UniProt |
---|---|---|---|---|---|---|---|---|
CHRNA10 | NM_020402.4 | c.1129G>A | p.Gly377Ser | missense_variant | Exon 5 of 5 | ENST00000250699.2 | NP_065135.2 | |
CHRNA10 | NM_001303034.2 | c.511G>A | p.Gly171Ser | missense_variant | Exon 5 of 5 | NP_001289963.1 | ||
CHRNA10 | NM_001303035.2 | c.511G>A | p.Gly171Ser | missense_variant | Exon 5 of 5 | NP_001289964.1 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | Exon rank | TSL | MANE | Protein | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|---|
CHRNA10 | ENST00000250699.2 | c.1129G>A | p.Gly377Ser | missense_variant | Exon 5 of 5 | 1 | NM_020402.4 | ENSP00000250699.2 | ||
CHRNA10 | ENST00000534359 | c.*210G>A | 3_prime_UTR_variant | Exon 5 of 5 | 1 | ENSP00000437107.1 | ||||
CHRNA10 | ENST00000526599.1 | n.*900G>A | non_coding_transcript_exon_variant | Exon 5 of 5 | 1 | ENSP00000432757.1 | ||||
CHRNA10 | ENST00000526599.1 | n.*900G>A | 3_prime_UTR_variant | Exon 5 of 5 | 1 | ENSP00000432757.1 |
Frequencies
GnomAD3 genomes AF: 0.00000657 AC: 1AN: 152246Hom.: 0 Cov.: 32
GnomAD3 exomes AF: 0.0000280 AC: 7AN: 249560Hom.: 0 AF XY: 0.0000148 AC XY: 2AN XY: 134986
GnomAD4 exome AF: 0.00000479 AC: 7AN: 1460944Hom.: 0 Cov.: 31 AF XY: 0.00000275 AC XY: 2AN XY: 726788
GnomAD4 genome AF: 0.00000657 AC: 1AN: 152246Hom.: 0 Cov.: 32 AF XY: 0.0000134 AC XY: 1AN XY: 74374
ClinVar
Submissions by phenotype
not specified Uncertain:1
The c.1129G>A (p.G377S) alteration is located in exon 5 (coding exon 5) of the CHRNA10 gene. This alteration results from a G to A substitution at nucleotide position 1129, causing the glycine (G) at amino acid position 377 to be replaced by a serine (S). 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