chr14-64421337-C-T

Position:

• chr14-64421337-C-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_005956.4(MTHFD1):​c.727+1412C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.911 in 152,270 control chromosomes in the GnomAD database, including 63,527 homozygotes. 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: 𝑓 0.91 (63527 hom., cov: 32)
• Consequence: MTHFD1 NM_005956.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.191

Genes affected

MTHFD1 (HGNC:7432): (methylenetetrahydrofolate dehydrogenase, cyclohydrolase and formyltetrahydrofolate synthetase 1) This gene encodes a protein that possesses three distinct enzymatic activities, 5,10-methylenetetrahydrofolate dehydrogenase, 5,10-methenyltetrahydrofolate cyclohydrolase and 10-formyltetrahydrofolate synthetase. Each of these activities catalyzes one of three sequential reactions in the interconversion of 1-carbon derivatives of tetrahydrofolate, which are substrates for methionine, thymidylate, and de novo purine syntheses. The trifunctional enzymatic activities are conferred by two major domains, an aminoterminal portion containing the dehydrogenase and cyclohydrolase activities and a larger synthetase domain. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.966 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
MTHFD1	NM_005956.4	c.727+1412C>T		intron_variant		ENST00000652337.1	NP_005947.3
MTHFD1	NM_001364837.1	c.727+1412C>T		intron_variant			NP_001351766.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
MTHFD1	ENST00000652337.1	c.727+1412C>T		intron_variant			NM_005956.4	ENSP00000498336	P1

Frequencies

GnomAD3 genomes AF: 0.911 AC: 138649 AN: 152152 Hom.: 63475 Cov.: 32

Gnomad AFR AF: 0.974

Gnomad AMI AF: 0.950

Gnomad AMR AF: 0.871

Gnomad ASJ AF: 0.910

Gnomad EAS AF: 0.664

Gnomad SAS AF: 0.957

Gnomad FIN AF: 0.885

Gnomad MID AF: 0.927

Gnomad NFE AF: 0.902

Gnomad OTH AF: 0.901

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.911 AC: 138759 AN: 152270 Hom.: 63527 Cov.: 32 AF XY: 0.909 AC XY: 67675 AN XY: 74446

Gnomad4 AFR AF: 0.974

Gnomad4 AMR AF: 0.870

Gnomad4 ASJ AF: 0.910

Gnomad4 EAS AF: 0.663

Gnomad4 SAS AF: 0.957

Gnomad4 FIN AF: 0.885

Gnomad4 NFE AF: 0.902

Gnomad4 OTH AF: 0.902

Alfa AF: 0.898 Hom.: 10105

Bravo AF: 0.908

Asia WGS AF: 0.838 AC: 2917 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	1.9
DANN	Benign	0.45

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

LitVar

Other links and lift over

dbSNP: rs1885031; hg19: chr14-64888055;