chr12-31981391-G-T

Variant names:

• chr12-31981391-G-T
• rs138851326
• NM_018169.4:c.436G>T

Variant summary

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

The NM_018169.4(RESF1):​c.436G>T​(p.Val146Leu) 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. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. V146I) has been classified as Uncertain significance.

• Frequency: Genomes: not found (cov: 32)
• Consequence: RESF1 NM_018169.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.29
• Publications: 0 publications found

Genes affected

RESF1 (HGNC:25559): (retroelement silencing factor 1) Predicted to enable histone binding activity and histone methyltransferase binding activity. Predicted to be involved in negative regulation of single stranded viral RNA replication via double stranded DNA intermediate and positive regulation of DNA methylation-dependent heterochromatin assembly. Predicted to act upstream of or within response to bacterium. Predicted to be located in nucleus. Predicted to colocalize with gamma-tubulin complex. [provided by Alliance of Genome Resources, Apr 2022]

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=0.018462181).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_018169.4. 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
	RESF1	NM_018169.4	MANE Select	c.436G>T	p.Val146Leu	missense	Exon 4 of 6	NP_060639.4	Q9HCM1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	RESF1	ENST00000312561.9	TSL:1 MANE Select	c.436G>T	p.Val146Leu	missense	Exon 4 of 6	ENSP00000310338.4	Q9HCM1
	RESF1	ENST00000913392.1		c.436G>T	p.Val146Leu	missense	Exon 2 of 4	ENSP00000583451.1
	RESF1	ENST00000913394.1		c.436G>T	p.Val146Leu	missense	Exon 5 of 7	ENSP00000583453.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD2 exomes AF: 0.0000120 AC: 3 AN: 250928 AF XY: 0.00

Gnomad AFR exome AF: 0.000186

Gnomad AMR exome AF: 0.00

Gnomad ASJ exome AF: 0.00

Gnomad EAS exome AF: 0.00

Gnomad FIN exome AF: 0.00

Gnomad NFE exome AF: 0.00

Gnomad OTH exome AF: 0.00

GnomAD4 exome Cov.: 44

GnomAD4 genome Cov.: 32

ExAC AF: 0.000585 AC: 71

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.098
BayesDel_addAF	Benign	-0.42	T
BayesDel_noAF	Benign	-0.61
CADD	Benign	0.0080
DANN	Benign	0.64
DEOGEN2	Benign	0.0084	T
Eigen	Benign	-1.8
Eigen_PC	Benign	-2.0
FATHMM_MKL	Benign	0.091	N
LIST_S2	Benign	0.48	T
M_CAP	Benign	0.0025	T
MetaRNN	Benign	0.018	T
MetaSVM	Benign	-1.0	T
MutationAssessor	Benign	0.34	N
PhyloP100		-1.3
PrimateAI	Benign	0.17	T
PROVEAN	Benign	-0.60	N
REVEL	Benign	0.045
Sift	Benign	0.33	T
Sift4G	Benign	0.44	T
Polyphen		0.0020	B
Vest4		0.032
MutPred		0.21		Gain of disorder (P = 0.1606)
MVP		0.048
MPC		0.0090
ClinPred		0.027	T
GERP RS		-11
Varity_R		0.024
gMVP		0.067
Mutation Taster		=97/3	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: rs138851326; hg19: chr12-32134325;