15-67779937-C-T

Position:

• chr15-67779937-C-T

Variant summary

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

The NM_145160.3(MAP2K5):​c.1242+7185C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.367 in 151,978 control chromosomes in the GnomAD database, including 11,014 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 0.37 (11014 hom., cov: 32)
• Consequence: MAP2K5 NM_145160.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.514

Genes affected

MAP2K5 (HGNC:6845): (mitogen-activated protein kinase kinase 5) The protein encoded by this gene is a dual specificity protein kinase that belongs to the MAP kinase kinase family. This kinase specifically interacts with and activates MAPK7/ERK5. This kinase itself can be phosphorylated and activated by MAP3K3/MEKK3, as well as by atypical protein kinase C isoforms (aPKCs). The signal cascade mediated by this kinase is involved in growth factor stimulated cell proliferation and muscle cell differentiation. Three alternatively spliced transcript variants of this gene encoding distinct isoforms have been described. [provided by RefSeq, May 2011]

MAP2K5 (HGNC:):

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 (EAS) allele frequency at 95% confidence interval = 0.672 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
MAP2K5	NM_145160.3	c.1242+7185C>T		intron_variant		ENST00000178640.10	NP_660143.1
MAP2K5	NM_002757.4	c.1212+7185C>T		intron_variant			NP_002748.1
MAP2K5	NM_001206804.2	c.1134+7185C>T		intron_variant			NP_001193733.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
MAP2K5	ENST00000178640.10	c.1242+7185C>T		intron_variant		1	NM_145160.3	ENSP00000178640.5

Frequencies

GnomAD3 genomes AF: 0.367 AC: 55711 AN: 151860 Hom.: 10972 Cov.: 32

Gnomad AFR AF: 0.356

Gnomad AMI AF: 0.189

Gnomad AMR AF: 0.529

Gnomad ASJ AF: 0.438

Gnomad EAS AF: 0.689

Gnomad SAS AF: 0.433

Gnomad FIN AF: 0.303

Gnomad MID AF: 0.342

Gnomad NFE AF: 0.316

Gnomad OTH AF: 0.384

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

GnomAD4 genome AF: 0.367 AC: 55804 AN: 151978 Hom.: 11014 Cov.: 32 AF XY: 0.373 AC XY: 27723 AN XY: 74298

Gnomad4 AFR AF: 0.357

Gnomad4 AMR AF: 0.530

Gnomad4 ASJ AF: 0.438

Gnomad4 EAS AF: 0.690

Gnomad4 SAS AF: 0.434

Gnomad4 FIN AF: 0.303

Gnomad4 NFE AF: 0.316

Gnomad4 OTH AF: 0.389

Alfa AF: 0.346 Hom.: 13421

Bravo AF: 0.388

Asia WGS AF: 0.584 AC: 2030 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	0.91
DANN	Benign	0.40

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: rs3784709; hg19: chr15-68072275;