chr3-69385716-T-G

Variant names:

• chr3-69385716-T-G
• rs17005789
• NM_015123.3:c.162+112A>C

Variant summary

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

The NM_015123.3(FRMD4B):​c.162+112A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0681 in 916,916 control chromosomes in the GnomAD database, including 2,882 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 0.066 (507 hom., cov: 32)
  • Exomes 𝑓: 0.069 (2375 hom.)
• Consequence: FRMD4B NM_015123.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.49
• Publications: 6 publications found

Genes affected

FRMD4B (HGNC:24886): (FERM domain containing 4B) This gene encodes a GRP1-binding protein which contains a FERM protein interaction domain as well as two coiled coil domains. This protein may play a role as a scaffolding protein. [provided by RefSeq, Mar 2014]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.8).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.178 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_015123.3. 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
	FRMD4B	NM_015123.3	MANE Select	c.162+112A>C		intron	N/A	NP_055938.2

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	FRMD4B	ENST00000398540.8	TSL:1 MANE Select	c.162+112A>C		intron	N/A	ENSP00000381549.3
	FRMD4B	ENST00000473188.5	TSL:1	n.477+112A>C		intron	N/A
	FRMD4B	ENST00000459638.5	TSL:5	c.-1+46918A>C		intron	N/A	ENSP00000417550.1

Frequencies

GnomAD3 genomes AF: 0.0659 AC: 10018 AN: 152118 Hom.: 505 Cov.: 32

Gnomad AFR AF: 0.0251

Gnomad AMI AF: 0.0384

Gnomad AMR AF: 0.150

Gnomad ASJ AF: 0.0738

Gnomad EAS AF: 0.136

Gnomad SAS AF: 0.187

Gnomad FIN AF: 0.0432

Gnomad MID AF: 0.0411

Gnomad NFE AF: 0.0611

Gnomad OTH AF: 0.0798

GnomAD4 exome AF: 0.0686 AC: 52445 AN: 764680 Hom.: 2375 AF XY: 0.0710 AC XY: 27063 AN XY: 381034

African (AFR) AF: 0.0223 AC: 376 AN: 16836

American (AMR) AF: 0.166 AC: 2407 AN: 14516

Ashkenazi Jewish (ASJ) AF: 0.0771 AC: 1104 AN: 14310

East Asian (EAS) AF: 0.0856 AC: 2376 AN: 27770

South Asian (SAS) AF: 0.160 AC: 6956 AN: 43548

European-Finnish (FIN) AF: 0.0423 AC: 1514 AN: 35768

Middle Eastern (MID) AF: 0.0617 AC: 151 AN: 2446

European-Non Finnish (NFE) AF: 0.0605 AC: 34740 AN: 574454

Other (OTH) AF: 0.0805 AC: 2821 AN: 35032

GnomAD4 genome AF: 0.0659 AC: 10032 AN: 152236 Hom.: 507 Cov.: 32 AF XY: 0.0693 AC XY: 5160 AN XY: 74426

African (AFR) AF: 0.0251 AC: 1043 AN: 41578

American (AMR) AF: 0.151 AC: 2306 AN: 15294

Ashkenazi Jewish (ASJ) AF: 0.0738 AC: 256 AN: 3470

East Asian (EAS) AF: 0.135 AC: 699 AN: 5162

South Asian (SAS) AF: 0.188 AC: 902 AN: 4806

European-Finnish (FIN) AF: 0.0432 AC: 458 AN: 10606

Middle Eastern (MID) AF: 0.0442 AC: 13 AN: 294

European-Non Finnish (NFE) AF: 0.0611 AC: 4153 AN: 68000

Other (OTH) AF: 0.0790 AC: 167 AN: 2114

Alfa AF: 0.0631 Hom.: 645

Bravo AF: 0.0703

Asia WGS AF: 0.141 AC: 488 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.80
CADD	Benign	0.94
DANN	Benign	0.54
PhyloP100		-1.5
PromoterAI		0.036	Neutral
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.12		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: rs17005789; hg19: chr3-69434867; COSMIC: COSV68332820;