NM_001492.6:c.-773G>C

Variant names:

• chr19-18884127-C-G
• NM_001492.6:c.-773G>C

Variant summary

Our verdict is Uncertain significance. Variant got 1 ACMG points: 2P and 1B. PM2 BP4

The NM_001492.6(GDF1):​c.-773G>C variant causes a 5 prime UTR premature start codon gain change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000000684 in 1,461,372 control chromosomes in the GnomAD database, with no homozygous occurrence. 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)
  • Exomes 𝑓: 6.8e-7 (0 hom.)
• Consequence: GDF1 NM_001492.6 5_prime_UTR_premature_start_codon_gain
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.53

Genes affected

GDF1 (HGNC:4214): (growth differentiation factor 1) This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. Studies in rodents suggest that this protein is involved in the establishment of left-right asymmetry in early embryogenesis and in neural development in later embryogenesis. The encoded protein is translated from a bicistronic mRNA that also encodes ceramide synthase 1. Mutations in this gene are associated with several congenital cardiovascular malformations. [provided by RefSeq, Jul 2016]

CERS1 (HGNC:14253): (ceramide synthase 1) This gene encodes a ceramide synthase enzyme, which catalyzes the synthesis of ceramide, the hydrophobic moiety of sphingolipids. The encoded enzyme synthesizes 18-carbon (C18) ceramide in brain neurons. Elevated expression of this gene may be associated with increased longevity, while decreased expression of this gene may be associated with myoclonus epilepsy with dementia in human patients. This protein is transcribed from a monocistronic mRNA as well as a bicistronic mRNA, which also encodes growth differentiation factor 1. [provided by RefSeq, Jul 2016]

ACMG classification

Verdict is Uncertain_significance. Variant got 1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.39298612).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
GDF1	NM_001492.6	c.-773G>C		5_prime_UTR_premature_start_codon_gain_variant	Exon 3 of 8	ENST00000247005.8	NP_001483.3
CERS1	NM_021267.5	c.550G>C	p.Val184Leu	missense_variant	Exon 3 of 8	ENST00000623882.4	NP_067090.1
GDF1	NM_001492.6	c.-773G>C		5_prime_UTR_variant	Exon 3 of 8	ENST00000247005.8	NP_001483.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
GDF1	ENST00000247005.8	c.-773G>C		5_prime_UTR_premature_start_codon_gain_variant	Exon 3 of 8	1	NM_001492.6	ENSP00000247005.5
CERS1	ENST00000623882.4	c.550G>C	p.Val184Leu	missense_variant	Exon 3 of 8	1	NM_021267.5	ENSP00000485308.1
GDF1	ENST00000247005.8	c.-773G>C		5_prime_UTR_variant	Exon 3 of 8	1	NM_001492.6	ENSP00000247005.5

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome AF: 6.84e-7 AC: 1 AN: 1461372 Hom.: 0 Cov.: 31 AF XY: 0.00 AC XY: 0 AN XY: 726932

Gnomad4 AFR exome AF: 0.00

Gnomad4 AMR exome AF: 0.00

Gnomad4 ASJ exome AF: 0.00

Gnomad4 EAS exome AF: 0.0000252

Gnomad4 SAS exome AF: 0.00

Gnomad4 FIN exome AF: 0.00

Gnomad4 NFE exome AF: 0.00

Gnomad4 OTH exome AF: 0.00

GnomAD4 genome Cov.: 31

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.15
BayesDel_addAF	Benign	0.010	T
BayesDel_noAF	Benign	-0.22
CADD	Benign	18
DANN	Benign	0.94
DEOGEN2	Uncertain	0.66	D;.;D
Eigen	Benign	-0.054
Eigen_PC	Benign	-0.0052
FATHMM_MKL	Uncertain	0.77	D
LIST_S2	Benign	0.83	T;T;D
M_CAP	Uncertain	0.096	D
MetaRNN	Benign	0.39	T;T;T
MetaSVM	Uncertain	-0.18	T
MutationAssessor	Benign	1.6	L;L;.
PrimateAI	Uncertain	0.54	T
PROVEAN	Benign	-1.4	.;N;N
REVEL	Uncertain	0.36
Sift	Benign	0.047	.;D;T
Sift4G	Benign	0.15	T;T;T
Polyphen		0.64	P;.;.
Vest4		0.38
MutPred		0.59		Gain of catalytic residue at V184 (P = 0.3174);Gain of catalytic residue at V184 (P = 0.3174);.;
MVP		0.64
ClinPred		0.55	D
GERP RS		4.4
Varity_R		0.19

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

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

Publications

No publications associated with this variant yet.

Other links and lift over

hg19: chr19-18994936;