rs11155762

Variant names:

• chr6-150951660-C-T
• rs11155762
• NM_015440.5:c.1726+2527C>T

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_015440.5(MTHFD1L):​c.1726+2527C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.3 in 152,094 control chromosomes in the GnomAD database, including 7,476 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 0.30 (7476 hom., cov: 32)
• Consequence: MTHFD1L NM_015440.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.606
• Publications: 1 publications found

Genes affected

MTHFD1L (HGNC:21055): (methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1 like) The protein encoded by this gene is involved in the synthesis of tetrahydrofolate (THF) in the mitochondrion. THF is important in the de novo synthesis of purines and thymidylate and in the regeneration of methionine from homocysteine. Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jun 2011]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.45 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
MTHFD1L	NM_015440.5	c.1726+2527C>T		intron_variant	Intron 16 of 27	ENST00000367321.8	NP_056255.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
MTHFD1L	ENST00000367321.8	c.1726+2527C>T		intron_variant	Intron 16 of 27	1	NM_015440.5	ENSP00000356290.3
MTHFD1L	ENST00000611279.4	c.1729+2527C>T		intron_variant	Intron 16 of 27	5		ENSP00000478253.1
MTHFD1L	ENST00000618312.4	c.1531+2527C>T		intron_variant	Intron 16 of 27	5		ENSP00000479539.1

Frequencies

GnomAD3 genomes AF: 0.300 AC: 45595 AN: 151976 Hom.: 7469 Cov.: 32

Gnomad AFR AF: 0.173

Gnomad AMI AF: 0.389

Gnomad AMR AF: 0.332

Gnomad ASJ AF: 0.264

Gnomad EAS AF: 0.465

Gnomad SAS AF: 0.258

Gnomad FIN AF: 0.397

Gnomad MID AF: 0.250

Gnomad NFE AF: 0.346

Gnomad OTH AF: 0.314

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

GnomAD4 genome AF: 0.300 AC: 45640 AN: 152094 Hom.: 7476 Cov.: 32 AF XY: 0.302 AC XY: 22449 AN XY: 74348

African (AFR) AF: 0.173 AC: 7179 AN: 41510

American (AMR) AF: 0.332 AC: 5076 AN: 15280

Ashkenazi Jewish (ASJ) AF: 0.264 AC: 914 AN: 3466

East Asian (EAS) AF: 0.466 AC: 2409 AN: 5170

South Asian (SAS) AF: 0.260 AC: 1254 AN: 4828

European-Finnish (FIN) AF: 0.397 AC: 4193 AN: 10560

Middle Eastern (MID) AF: 0.265 AC: 78 AN: 294

European-Non Finnish (NFE) AF: 0.346 AC: 23521 AN: 67968

Other (OTH) AF: 0.314 AC: 662 AN: 2108

Alfa AF: 0.306 Hom.: 965

Bravo AF: 0.291

Asia WGS AF: 0.331 AC: 1149 AN: 3466

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	3.7
DANN	Benign	0.48
PhyloP100		-0.61
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs11155762; hg19: chr6-151272796;