5-137949093-G-C

Variant names:

• chr5-137949093-G-C
• NM_001385994.1:c.2022C>G

Variant summary

Our verdict is Likely benign. Variant got -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_001385994.1(FAM13B):​c.2022C>G​(p.Asp674Glu) 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. 13/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).

• Frequency: Genomes: not found (cov: 32)
• Consequence: FAM13B NM_001385994.1 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 1.08

Genes affected

FAM13B (HGNC:1335): (family with sequence similarity 13 member B) Predicted to enable GTPase activator activity. Predicted to be involved in regulation of small GTPase mediated signal transduction. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Likely_benign. Variant got -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.061363965).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
FAM13B	NM_001385994.1	c.2022C>G	p.Asp674Glu	missense_variant	Exon 18 of 24	ENST00000689681.1	NP_001372923.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
FAM13B	ENST00000689681.1	c.2022C>G	p.Asp674Glu	missense_variant	Exon 18 of 24		NM_001385994.1	ENSP00000509788.1
FAM13B	ENST00000033079.7	c.1956C>G	p.Asp652Glu	missense_variant	Exon 17 of 23	1		ENSP00000033079.3
FAM13B	ENST00000420893.6	c.1956C>G	p.Asp652Glu	missense_variant	Exon 17 of 22	1		ENSP00000388521.2
FAM13B	ENST00000425075.6	c.1668C>G	p.Asp556Glu	missense_variant	Exon 17 of 22	1		ENSP00000394669.2

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 32

GnomAD4 genome Cov.: 32

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

Submissions by phenotype

not specified Uncertain:1

Jun 17, 2024

Ambry Genetics

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

The c.1956C>G (p.D652E) alteration is located in exon 17 (coding exon 15) of the FAM13B gene. This alteration results from a C to G substitution at nucleotide position 1956, causing the aspartic acid (D) at amino acid position 652 to be replaced by a glutamic acid (E). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.14
BayesDel_addAF	Benign	-0.35	T
BayesDel_noAF	Benign	-0.74
CADD	Benign	19
DANN	Uncertain	0.99
DEOGEN2	Benign	0.018	T;.;.
Eigen	Benign	-0.51
Eigen_PC	Benign	-0.28
FATHMM_MKL	Uncertain	0.85	D
LIST_S2	Benign	0.69	T;T;T
M_CAP	Benign	0.0033	T
MetaRNN	Benign	0.061	T;T;T
MetaSVM	Benign	-1.0	T
MutationAssessor	Benign	-0.32	N;.;N
PrimateAI	Uncertain	0.55	T
PROVEAN	Benign	-0.12	N;N;N
REVEL	Benign	0.11
Sift	Benign	1.0	T;T;T
Sift4G	Benign	1.0	T;T;T
Polyphen		0.0070	B;.;B
Vest4		0.26
MutPred		0.047		Loss of stability (P = 0.1553);.;Loss of stability (P = 0.1553);
MVP		0.13
MPC		0.12
ClinPred		0.29	T
GERP RS		4.2
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.7
Varity_R		0.030
gMVP		0.042

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.040		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

No publications associated with this variant yet.

Other links and lift over

hg19: chr5-137284782;