chr14-94288518-C-T
Variant summary
Our verdict is Uncertain significance. Variant got 1 ACMG points: 2P and 1B. PM2BP4
The NM_001100607.3(SERPINA10):c.760G>A(p.Asp254Asn) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000205 in 1,461,892 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. 14/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).
Frequency
Consequence
NM_001100607.3 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 |
---|---|---|---|---|---|---|---|
SERPINA10 | NM_001100607.3 | c.760G>A | p.Asp254Asn | missense_variant | 3/5 | ENST00000261994.9 | |
SERPINA10 | NM_016186.3 | c.760G>A | p.Asp254Asn | missense_variant | 3/5 | ||
SERPINA10 | XM_017021353.2 | c.880G>A | p.Asp294Asn | missense_variant | 4/6 | ||
SERPINA10 | XM_005267733.6 | c.760G>A | p.Asp254Asn | missense_variant | 3/5 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
SERPINA10 | ENST00000261994.9 | c.760G>A | p.Asp254Asn | missense_variant | 3/5 | 1 | NM_001100607.3 | A2 | |
SERPINA10 | ENST00000554723.5 | c.880G>A | p.Asp294Asn | missense_variant | 3/5 | 1 | P4 | ||
SERPINA10 | ENST00000393096.5 | c.760G>A | p.Asp254Asn | missense_variant | 3/5 | 1 | A2 | ||
SERPINA10 | ENST00000554173.1 | c.760G>A | p.Asp254Asn | missense_variant | 2/4 | 1 | A2 |
Frequencies
GnomAD3 genomes Cov.: 32
GnomAD3 exomes AF: 0.00000398 AC: 1AN: 251366Hom.: 0 AF XY: 0.00000736 AC XY: 1AN XY: 135874
GnomAD4 exome AF: 0.00000205 AC: 3AN: 1461892Hom.: 0 Cov.: 32 AF XY: 0.00000413 AC XY: 3AN XY: 727248
GnomAD4 genome Cov.: 32
ClinVar
Submissions by phenotype
not specified Uncertain:1
Uncertain significance, criteria provided, single submitter | clinical testing | Ambry Genetics | Mar 07, 2024 | The c.760G>A (p.D254N) alteration is located in exon 3 (coding exon 2) of the SERPINA10 gene. This alteration results from a G to A substitution at nucleotide position 760, causing the aspartic acid (D) at amino acid position 254 to be replaced by an asparagine (N). 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