rs7887

Variant names:

• chr6-31896770-G-C
• rs7887
• NM_006709.5:c.164C>G

Your query was ambiguous. Multiple possible variants found:

• chr6-31896770-G-C
• chr6-31896770-G-T

Variant summary

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

The NM_006709.5(EHMT2):​c.164C>G​(p.Thr55Ser) variant causes a missense 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. 16/22 in silico tools predict 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: EHMT2 NM_006709.5 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.33
• Publications: 48 publications found

Genes affected

EHMT2 (HGNC:14129): (euchromatic histone lysine methyltransferase 2) This gene encodes a methyltransferase that methylates lysine residues of histone H3. Methylation of H3 at lysine 9 by this protein results in recruitment of additional epigenetic regulators and repression of transcription. This gene was initially thought to be two different genes, NG36 and G9a, adjacent to each other in the HLA locus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]

EHMT2 Gene-Disease associations (from GenCC):

• neurodevelopmental disorder

  Inheritance: AR Classification: LIMITED Submitted by: Ambry Genetics

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 (MetaRNN=0.022219718).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_006709.5. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	EHMT2	NM_006709.5	MANE Select	c.164C>G	p.Thr55Ser	missense	Exon 3 of 28	NP_006700.3
	EHMT2	NM_001363689.2		c.335C>G	p.Thr112Ser	missense	Exon 2 of 27	NP_001350618.1
	EHMT2	NM_001289413.2		c.335C>G	p.Thr112Ser	missense	Exon 2 of 26	NP_001276342.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	EHMT2	ENST00000375537.9	TSL:1 MANE Select	c.164C>G	p.Thr55Ser	missense	Exon 3 of 28	ENSP00000364687.4
	EHMT2	ENST00000395728.7	TSL:1	c.335C>G	p.Thr112Ser	missense	Exon 2 of 27	ENSP00000379078.3
	EHMT2	ENST00000375528.8	TSL:2	c.335C>G	p.Thr112Ser	missense	Exon 2 of 26	ENSP00000364678.4

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 55

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.058
BayesDel_addAF	Benign	-0.42	T
BayesDel_noAF	Benign	-0.83
CADD	Benign	0.25
DANN	Benign	0.45
DEOGEN2	Benign	0.025	T
Eigen	Benign	-1.7
Eigen_PC	Benign	-1.8
FATHMM_MKL	Benign	0.12	N
M_CAP	Benign	0.0067	T
MetaRNN	Benign	0.022	T
MetaSVM	Benign	-1.0	T
MutationAssessor	Benign	0.0	N
PhyloP100		-1.3
PrimateAI	Benign	0.41	T
PROVEAN	Benign	-0.30	N
REVEL	Benign	0.033
Sift	Benign	0.64	T
Sift4G	Benign	0.43	T
Polyphen		0.0	B
Vest4		0.038
MutPred		0.10		Gain of glycosylation at P113 (P = 0.14)
MVP		0.26
MPC		0.44
ClinPred		0.16	T
GERP RS		-6.0
PromoterAI		-0.033	Neutral
RBP_binding_hub_radar		1.0
RBP_regulation_power_radar		2.7
Varity_R		0.037
gMVP		0.031
Mutation Taster		=96/4	polymorphism

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: rs7887; hg19: chr6-31864547;