NM_003748.4:c.1583C>G

Variant names:

• chr1-18872954-G-C
• rs61757683
• NM_003748.4:c.1583C>G

Variant summary

Our verdict is Uncertain significance. The variant received 2 ACMG points: 2P and 0B. PM2

The NM_003748.4(ALDH4A1):​c.1583C>G​(p.Thr528Ser) variant causes a missense change involving the alteration of a conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. T528N) has been classified as Likely benign.

• Frequency: Genomes: not found (cov: 33)
• Consequence: ALDH4A1 NM_003748.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 9.74
• Publications: 15 publications found

Genes affected

ALDH4A1 (HGNC:406): (aldehyde dehydrogenase 4 family member A1) This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jun 2009]

ALDH4A1 Gene-Disease associations (from GenCC):

• hyperprolinemia type 2

  Inheritance: AR Classification: DEFINITIVE, STRONG, SUPPORTIVE, LIMITED Submitted by: Ambry Genetics, Labcorp Genetics (formerly Invitae), G2P, ClinGen, Orphanet

ACMG classification

Our verdict: Uncertain_significance. The variant received 2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ALDH4A1	NM_003748.4	c.1583C>G	p.Thr528Ser	missense_variant	Exon 15 of 15	ENST00000375341.8	NP_003739.2
ALDH4A1	NM_170726.3	c.1583C>G	p.Thr528Ser	missense_variant	Exon 15 of 16		NP_733844.1
ALDH4A1	NM_001319218.2	c.1430C>G	p.Thr477Ser	missense_variant	Exon 14 of 14		NP_001306147.1
ALDH4A1	NM_001161504.2	c.1403C>G	p.Thr468Ser	missense_variant	Exon 15 of 15		NP_001154976.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ALDH4A1	ENST00000375341.8	c.1583C>G	p.Thr528Ser	missense_variant	Exon 15 of 15	1	NM_003748.4	ENSP00000364490.3
ALDH4A1	ENST00000290597.9	c.1583C>G	p.Thr528Ser	missense_variant	Exon 15 of 16	1		ENSP00000290597.5
ALDH4A1	ENST00000538839.5	c.1430C>G	p.Thr477Ser	missense_variant	Exon 14 of 14	1		ENSP00000446071.1
ALDH4A1	ENST00000538309.5	c.1403C>G	p.Thr468Ser	missense_variant	Exon 15 of 15	2		ENSP00000442988.1

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 33

Alfa AF: 0.00 Hom.: 132

Bravo AF: 0.00000378

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	0.62
BayesDel_addAF	Pathogenic	0.20	D
BayesDel_noAF	Uncertain	0.040
CADD	Pathogenic	33
DANN	Uncertain	1.0
DEOGEN2	Uncertain	0.51	D;.;D;.
Eigen	Pathogenic	0.81
Eigen_PC	Pathogenic	0.73
FATHMM_MKL	Pathogenic	0.99	D
LIST_S2	Uncertain	0.96	.;D;D;D
M_CAP	Benign	0.072	D
MetaRNN	Uncertain	0.64	D;D;D;D
MetaSVM	Uncertain	0.53	D
MutationAssessor	Pathogenic	3.4	M;.;M;.
PhyloP100		9.7
PrimateAI	Uncertain	0.66	T
PROVEAN	Uncertain	-3.2	D;D;D;D
REVEL	Uncertain	0.61
Sift	Uncertain	0.0030	D;D;D;D
Sift4G	Uncertain	0.018	D;D;D;D
Polyphen		0.95	P;.;P;.
Vest4		0.70
MutPred		0.71		Gain of ubiquitination at K531 (P = 0.0737);.;Gain of ubiquitination at K531 (P = 0.0737);.;
MVP		0.92
MPC		0.14
ClinPred		0.98	D
GERP RS		4.8
Varity_R		0.65
gMVP		0.63
Mutation Taster		=20/80	disease causing

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.46		Details are displayed if max score is > 0.2
DS_AG_spliceai		0.46		Position offset: -1

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

Other links and lift over

dbSNP: rs61757683; hg19: chr1-19199448;