rs6731176

Variant names:

• chr2-127313427-C-A
• rs6731176
• NM_001371910.2:c.1456+1327G>T

Your query was ambiguous. Multiple possible variants found:

• chr2-127313427-C-A
• chr2-127313427-C-G
• chr2-127313427-C-T

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_001371910.2(MAP3K2):​c.1456+1327G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. 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: not found (cov: 32)
• Consequence: MAP3K2 NM_001371910.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.56
• Publications: 18 publications found

Genes affected

MAP3K2 (HGNC:6854): (mitogen-activated protein kinase kinase kinase 2) The protein encoded by this gene is a member of serine/threonine protein kinase family. This kinase preferentially activates other kinases involved in the MAP kinase signaling pathway. This kinase has been shown to directly phosphorylate and activate Ikappa B kinases, and thus plays a role in NF-kappa B signaling pathway. This kinase has also been found to bind and activate protein kinase C-related kinase 2, which suggests its involvement in a regulated signaling process. [provided by RefSeq, Jul 2008]

ENSG00000286145 (HGNC:):

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001371910.2. 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
	MAP3K2	NM_001371910.2	MANE Select	c.1456+1327G>T		intron	N/A	NP_001358839.1	Q9Y2U5
	MAP3K2	NM_001371911.1		c.1456+1327G>T		intron	N/A	NP_001358840.1	Q9Y2U5
	MAP3K2	NM_006609.5		c.1456+1327G>T		intron	N/A	NP_006600.3

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	MAP3K2	ENST00000682094.1	MANE Select	c.1456+1327G>T		intron	N/A	ENSP00000507315.1	Q9Y2U5
	MAP3K2	ENST00000344908.9	TSL:1	c.1456+1327G>T		intron	N/A	ENSP00000343463.5	Q9Y2U5
	MAP3K2	ENST00000409947.5	TSL:1	c.1456+1327G>T		intron	N/A	ENSP00000387246.1	Q9Y2U5

Frequencies

GnomAD3 genomes Cov.: 32

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

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	0.028
DANN	Benign	0.69
PhyloP100		-2.6

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: rs6731176; hg19: chr2-128071003;