NM_004059.5:c.439-19A>C
Variant summary
Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2BP4_Strong
The NM_004059.5(KYAT1):c.439-19A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.
Frequency
Consequence
NM_004059.5 intron
Scores
Clinical Significance
Conservation
Publications
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ACMG classification
Our verdict: Likely_benign. The variant received -2 ACMG points.
Variant Effect in Transcripts
ACMG analysis was done for transcript: NM_004059.5. You can select a different transcript below to see updated ACMG assignments.
RefSeq Transcripts
| Selected | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| KYAT1 | NM_004059.5 | MANE Select | c.439-19A>C | intron | N/A | NP_004050.3 | |||
| KYAT1-SPOUT1 | NM_001414398.1 | c.439-19A>C | intron | N/A | NP_001401327.1 | ||||
| KYAT1 | NM_001287390.3 | c.721-19A>C | intron | N/A | NP_001274319.1 |
Ensembl Transcripts
| Selected | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| KYAT1 | ENST00000302586.8 | TSL:1 MANE Select | c.439-19A>C | intron | N/A | ENSP00000302227.3 | |||
| KYAT1 | ENST00000651925.1 | c.718-19A>C | intron | N/A | ENSP00000498386.1 | ||||
| KYAT1 | ENST00000462722.5 | TSL:1 | n.585-19A>C | intron | N/A |
Frequencies
GnomAD3 genomes Cov.: 31
GnomAD4 exome Cov.: 42
GnomAD4 genome Cov.: 31
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at