rs397518006

Positions:

• chr1-216246662-G-A
• chr1-216246662-G-T

Variant summary

Our verdict is Uncertain significance. Variant got 3 ACMG points: 4P and 1B. PM1 PM2 BP4

The NM_206933.4(USH2A):​c.2732C>T​(p.Thr911Ile) 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. 15/21 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. T911N) has been classified as Likely benign.

• Frequency: Genomes: not found (cov: 32)
• Consequence: USH2A NM_206933.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 2.41

Genes affected

USH2A (HGNC:12601): (usherin) This gene encodes a protein that contains laminin EGF motifs, a pentaxin domain, and many fibronectin type III motifs. The protein is found in the basement membrane, and may be important in development and homeostasis of the inner ear and retina. Mutations within this gene have been associated with Usher syndrome type IIa and retinitis pigmentosa. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]

ACMG classification

Verdict is Uncertain_significance. Variant got 3 ACMG points.

• PM1: In a domain Laminin EGF-like 8 (size 50) in uniprot entity USH2A_HUMAN there are 13 pathogenic changes around while only 4 benign (76%) in NM_206933.4
• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.31566972).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
USH2A	NM_206933.4	c.2732C>T	p.Thr911Ile	missense_variant	13/72	ENST00000307340.8	NP_996816.3
USH2A	NM_007123.6	c.2732C>T	p.Thr911Ile	missense_variant	13/21		NP_009054.6

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
USH2A	ENST00000307340.8	c.2732C>T	p.Thr911Ile	missense_variant	13/72	1	NM_206933.4	ENSP00000305941.3
USH2A	ENST00000366942.3	c.2732C>T	p.Thr911Ile	missense_variant	13/21	1		ENSP00000355909.3
USH2A	ENST00000674083.1	c.2732C>T	p.Thr911Ile	missense_variant	13/73			ENSP00000501296.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.18
BayesDel_addAF	Benign	-0.11	T
BayesDel_noAF	Benign	-0.39
CADD	Benign	15
DANN	Uncertain	1.0
DEOGEN2	Benign	0.048	T;.
Eigen	Benign	0.037
Eigen_PC	Benign	0.0023
FATHMM_MKL	Uncertain	0.91	D
LIST_S2	Benign	0.56	T;T
M_CAP	Benign	0.055	D
MetaRNN	Benign	0.32	T;T
MetaSVM	Benign	-0.77	T
MutationAssessor	Benign	1.9	L;L
PrimateAI	Benign	0.35	T
PROVEAN	Benign	-1.9	N;N
REVEL	Benign	0.20
Sift	Uncertain	0.025	D;D
Sift4G	Uncertain	0.0040	D;D
Polyphen		0.94	P;P
Vest4		0.32
MutPred		0.45		Loss of disorder (P = 0.0647);Loss of disorder (P = 0.0647);
MVP		0.94
MPC		0.034
ClinPred		0.62	D
GERP RS		3.1
Varity_R		0.12
gMVP		0.43

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

Publications

LitVar

Other links and lift over

dbSNP: rs397518006; hg19: chr1-216420004;