NM_174938.6:c.295+10552T>C

Variant names:

• chr9-83362361-A-G
• rs7035160
• NM_174938.6:c.295+10552T>C

Variant summary

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

The NM_174938.6(FRMD3):​c.295+10552T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.612 in 152,068 control chromosomes in the GnomAD database, including 28,805 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 0.61 (28805 hom., cov: 32)
• Consequence: FRMD3 NM_174938.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.97
• Publications: 5 publications found

Genes affected

FRMD3 (HGNC:24125): (FERM domain containing 3) The protein encoded by this gene is a single pass membrane protein primarily found in ovaries. A similar protein in erythrocytes helps determine the shape of red blood cells, but the function of the encoded protein has not been determined. There is some evidence that this is a tumor suppressor gene, and there is also evidence linking defects in this gene to susceptibility to diabetic nephropathy in type 1 diabetes. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.615 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
FRMD3	NM_174938.6	c.295+10552T>C		intron_variant	Intron 3 of 13	ENST00000304195.8	NP_777598.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
FRMD3	ENST00000304195.8	c.295+10552T>C		intron_variant	Intron 3 of 13	1	NM_174938.6	ENSP00000303508.3
FRMD3	ENST00000621208.4	c.163+10552T>C		intron_variant	Intron 3 of 13	1		ENSP00000484839.1
FRMD3	ENST00000376438.5	c.295+10552T>C		intron_variant	Intron 3 of 14	2		ENSP00000365621.1

Frequencies

GnomAD3 genomes AF: 0.612 AC: 93036 AN: 151950 Hom.: 28769 Cov.: 32

Gnomad AFR AF: 0.614

Gnomad AMI AF: 0.542

Gnomad AMR AF: 0.621

Gnomad ASJ AF: 0.548

Gnomad EAS AF: 0.377

Gnomad SAS AF: 0.526

Gnomad FIN AF: 0.724

Gnomad MID AF: 0.582

Gnomad NFE AF: 0.620

Gnomad OTH AF: 0.611

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

GnomAD4 genome AF: 0.612 AC: 93114 AN: 152068 Hom.: 28805 Cov.: 32 AF XY: 0.613 AC XY: 45564 AN XY: 74330

African (AFR) AF: 0.614 AC: 25465 AN: 41478

American (AMR) AF: 0.622 AC: 9497 AN: 15280

Ashkenazi Jewish (ASJ) AF: 0.548 AC: 1901 AN: 3468

East Asian (EAS) AF: 0.377 AC: 1942 AN: 5156

South Asian (SAS) AF: 0.527 AC: 2541 AN: 4820

European-Finnish (FIN) AF: 0.724 AC: 7672 AN: 10590

Middle Eastern (MID) AF: 0.582 AC: 171 AN: 294

European-Non Finnish (NFE) AF: 0.620 AC: 42157 AN: 67970

Other (OTH) AF: 0.606 AC: 1276 AN: 2104

Alfa AF: 0.618 Hom.: 49789

Bravo AF: 0.604

Asia WGS AF: 0.483 AC: 1681 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	0.066
DANN	Benign	0.49
PhyloP100		-2.0
Mutation Taster		=100/0	polymorphism (auto)

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: rs7035160; hg19: chr9-85977276;