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

Genomes: not found (cov: 31)

Consequence

KYAT1
NM_004059.5 intron

Scores

2

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: -0.486

Publications

12 publications found
Variant links:
Genes affected
KYAT1 (HGNC:1564): (kynurenine aminotransferase 1) This gene encodes a cytosolic enzyme that is responsible for the metabolism of cysteine conjugates of certain halogenated alkenes and alkanes. This metabolism can form reactive metabolites leading to nephrotoxicity and neurotoxicity. Increased levels of this enzyme have been linked to schizophrenia. Multiple transcript variants that encode different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]

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ACMG classification

Classification was made for transcript

Our verdict: Likely_benign. The variant received -2 ACMG points.

PM2
Very rare variant in population databases, with high coverage;
BP4
Computational evidence support a benign effect (BayesDel_noAF=-0.92).

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
GeneTranscriptTagsHGVScHGVSpEffectExon RankProteinUniProt
KYAT1
NM_004059.5
MANE Select
c.439-19A>C
intron
N/ANP_004050.3
KYAT1-SPOUT1
NM_001414398.1
c.439-19A>C
intron
N/ANP_001401327.1
KYAT1
NM_001287390.3
c.721-19A>C
intron
N/ANP_001274319.1

Ensembl Transcripts

Selected
GeneTranscriptTagsHGVScHGVSpEffectExon RankProteinUniProt
KYAT1
ENST00000302586.8
TSL:1 MANE Select
c.439-19A>C
intron
N/AENSP00000302227.3
KYAT1
ENST00000651925.1
c.718-19A>C
intron
N/AENSP00000498386.1
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 in ClinVar

Computational scores

Source: dbNSFP v4.9

Name
Calibrated prediction
Score
Prediction
BayesDel_noAF
Benign
-0.92
CADD
Benign
0.46
DANN
Benign
0.44
PhyloP100
-0.49

Splicing

Name
Calibrated prediction
Score
Prediction
SpliceAI score (max)
0.010
Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

Other links and lift over

dbSNP: rs2280841; hg19: chr9-131600111; API