rs1549854

chr15-66404397-A-Cchr15-66404397-A-G

Variant summary

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

The NM_002755.4(MAP2K1):c.80+16970A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.443 in 151,962 control chromosomes in the GnomAD database, including 15,563 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 0.44 (15563 hom., cov: 31)
• Consequence: MAP2K1 NM_002755.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.349

Genes affected

MAP2K1 (HGNC:6840): (mitogen-activated protein kinase kinase 1) The protein encoded by this gene is a member of the dual specificity protein kinase family, which acts as a mitogen-activated protein (MAP) kinase kinase. MAP kinases, also known as extracellular signal-regulated kinases (ERKs), act as an integration point for multiple biochemical signals. This protein kinase lies upstream of MAP kinases and stimulates the enzymatic activity of MAP kinases upon wide variety of extra- and intracellular signals. As an essential component of MAP kinase signal transduction pathway, this kinase is involved in many cellular processes such as proliferation, differentiation, transcription regulation and development. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.516 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
MAP2K1	NM_002755.4	c.80+16970A>C		intron_variant		ENST00000307102.10
MAP2K1	NM_001411065.1	c.14+2450A>C		intron_variant
MAP2K1	XM_011521783.4	c.14+2450A>C		intron_variant
MAP2K1	XM_017022411.3	c.80+16970A>C		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
MAP2K1	ENST00000307102.10	c.80+16970A>C		intron_variant		1	NM_002755.4	P1

Frequencies

GnomAD3 genomes AF: 0.443 AC: 67191 AN: 151844 Hom.: 15533 Cov.: 31

Gnomad AFR AF: 0.338

Gnomad AMI AF: 0.402

Gnomad AMR AF: 0.524

Gnomad ASJ AF: 0.363

Gnomad EAS AF: 0.448

Gnomad SAS AF: 0.461

Gnomad FIN AF: 0.456

Gnomad MID AF: 0.326

Gnomad NFE AF: 0.489

Gnomad OTH AF: 0.439

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

GnomAD4 genome AF: 0.443 AC: 67269 AN: 151962 Hom.: 15563 Cov.: 31 AF XY: 0.444 AC XY: 32977 AN XY: 74258

Gnomad4 AFR AF: 0.338

Gnomad4 AMR AF: 0.525

Gnomad4 ASJ AF: 0.363

Gnomad4 EAS AF: 0.449

Gnomad4 SAS AF: 0.462

Gnomad4 FIN AF: 0.456

Gnomad4 NFE AF: 0.489

Gnomad4 OTH AF: 0.440

Alfa AF: 0.475 Hom.: 9646

Bravo AF: 0.444

Asia WGS AF: 0.430 AC: 1500 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
Cadd	Benign	1.7
Dann	Benign	0.43

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: rs1549854; hg19: chr15-66696735;