NM_004721.5:c.-86+31503A>G

Variant names:

• chr3-185394871-A-G
• rs4687299
• NM_004721.5:c.-86+31503A>G

Variant summary

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

The NM_004721.5(MAP3K13):​c.-86+31503A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.703 in 151,898 control chromosomes in the GnomAD database, including 38,082 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 0.70 (38082 hom., cov: 30)
• Consequence: MAP3K13 NM_004721.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.891
• Publications: 3 publications found

Genes affected

MAP3K13 (HGNC:6852): (mitogen-activated protein kinase kinase kinase 13) The protein encoded by this gene is a member of serine/threonine protein kinase family. This kinase contains a dual leucine-zipper motif, and has been shown to form dimers/oligomers through its leucine-zipper motif. This kinase can phosphorylate and activate MAPK8/JNK, MAP2K7/MKK7, which suggests a role in the JNK signaling pathway. [provided by RefSeq, Jul 2008]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.78).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.767 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_004721.5. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	MAP3K13	NM_004721.5	MANE Select	c.-86+31503A>G		intron	N/A	NP_004712.1	O43283-1
	MAP3K13	NM_001242314.2		c.-85-33626A>G		intron	N/A	NP_001229243.1	O43283-1
	MAP3K13	NM_001242317.2		c.39-48574A>G		intron	N/A	NP_001229246.1	O43283-5

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	MAP3K13	ENST00000265026.8	TSL:1 MANE Select	c.-86+31503A>G		intron	N/A	ENSP00000265026.3	O43283-1
	MAP3K13	ENST00000424227.5	TSL:1	c.-85-33626A>G		intron	N/A	ENSP00000399910.1	O43283-1
	MAP3K13	ENST00000433092.5	TSL:1	n.-85-33626A>G		intron	N/A	ENSP00000389798.1	O43283-6

Frequencies

GnomAD3 genomes AF: 0.703 AC: 106653 AN: 151780 Hom.: 38059 Cov.: 30

Gnomad AFR AF: 0.560

Gnomad AMI AF: 0.874

Gnomad AMR AF: 0.708

Gnomad ASJ AF: 0.809

Gnomad EAS AF: 0.672

Gnomad SAS AF: 0.748

Gnomad FIN AF: 0.740

Gnomad MID AF: 0.736

Gnomad NFE AF: 0.773

Gnomad OTH AF: 0.726

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

GnomAD4 genome AF: 0.703 AC: 106715 AN: 151898 Hom.: 38082 Cov.: 30 AF XY: 0.702 AC XY: 52124 AN XY: 74240

African (AFR) AF: 0.560 AC: 23168 AN: 41384

American (AMR) AF: 0.708 AC: 10810 AN: 15258

Ashkenazi Jewish (ASJ) AF: 0.809 AC: 2807 AN: 3470

East Asian (EAS) AF: 0.673 AC: 3472 AN: 5160

South Asian (SAS) AF: 0.749 AC: 3613 AN: 4824

European-Finnish (FIN) AF: 0.740 AC: 7784 AN: 10518

Middle Eastern (MID) AF: 0.747 AC: 218 AN: 292

European-Non Finnish (NFE) AF: 0.773 AC: 52510 AN: 67968

Other (OTH) AF: 0.728 AC: 1538 AN: 2114

Alfa AF: 0.751 Hom.: 33958

Bravo AF: 0.692

Asia WGS AF: 0.687 AC: 2385 AN: 3470

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.78
CADD	Benign	5.6
DANN	Benign	0.89
PhyloP100		0.89
Mutation Taster		=99/1	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: rs4687299; hg19: chr3-185112659;