chr11-2164326-G-T

Position:

• chr11-2164326-G-T

Variant summary

Our verdict is Uncertain significance. Variant got 1 ACMG points: 2P and 1B. PM2 BP4

The NM_000360.4(TH):​c.1401C>A​(p.Asp467Glu) 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: 33)
• Consequence: TH NM_000360.4 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: -1.16

Genes affected

TH (HGNC:11782): (tyrosine hydroxylase) The protein encoded by this gene is involved in the conversion of tyrosine to dopamine. It is the rate-limiting enzyme in the synthesis of catecholamines, hence plays a key role in the physiology of adrenergic neurons. Mutations in this gene have been associated with autosomal recessive Segawa syndrome. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Uncertain_significance. Variant got 1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.27184343).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
TH	NM_000360.4	c.1401C>A	p.Asp467Glu	missense_variant	13/13	ENST00000352909.8	NP_000351.2
TH	NM_199292.3	c.1494C>A	p.Asp498Glu	missense_variant	14/14		NP_954986.2
TH	NM_199293.3	c.1482C>A	p.Asp494Glu	missense_variant	14/14		NP_954987.2
TH	XM_011520335.3	c.1413C>A	p.Asp471Glu	missense_variant	13/13		XP_011518637.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
TH	ENST00000352909.8	c.1401C>A	p.Asp467Glu	missense_variant	13/13	1	NM_000360.4	ENSP00000325951.4
TH	ENST00000381178.5	c.1494C>A	p.Asp498Glu	missense_variant	14/14	1		ENSP00000370571.1
TH	ENST00000381175.5	c.1482C>A	p.Asp494Glu	missense_variant	14/14	1		ENSP00000370567.1
TH	ENST00000333684.9	c.1119C>A	p.Asp373Glu	missense_variant	11/11	1		ENSP00000328814.6

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 33

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

Submissions by phenotype

Autosomal recessive DOPA responsive dystonia Uncertain:1

Uncertain significance, criteria provided, single submitter

clinical testing

Labcorp Genetics (formerly Invitae), Labcorp

Jun 27, 2022

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. This variant disrupts the p.Asp498 amino acid residue in TH. Other variant(s) that disrupt this residue have been determined to be pathogenic (PMID: 11160968, 15505183, 15747353, 24753243). This suggests that this residue is clinically significant, and that variants that disrupt this residue are likely to be disease-causing. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt TH protein function. This variant has not been reported in the literature in individuals affected with TH-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces aspartic acid, which is acidic and polar, with glutamic acid, which is acidic and polar, at codon 498 of the TH protein (p.Asp498Glu). -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.095
BayesDel_addAF	Benign	-0.067	T
BayesDel_noAF	Benign	-0.33
CADD	Benign	0.0030
DANN	Benign	0.73
DEOGEN2	Uncertain	0.57	D;.;.;.
Eigen	Benign	-1.9
Eigen_PC	Benign	-1.9
FATHMM_MKL	Benign	0.13	N
LIST_S2	Benign	0.82	T;T;T;T
M_CAP	Pathogenic	0.72	D
MetaRNN	Benign	0.27	T;T;T;T
MetaSVM	Uncertain	0.56	D
MutationAssessor	Benign	-1.3	N;.;.;.
PrimateAI	Uncertain	0.58	T
PROVEAN	Benign	1.1	N;N;.;N
REVEL	Uncertain	0.30
Sift	Benign	1.0	T;T;.;T
Sift4G	Benign	1.0	T;T;T;T
Polyphen		0.0020	B;B;.;B
Vest4		0.023
MutPred		0.55		Loss of catalytic residue at D501 (P = 0.1139);.;.;.;
MVP		0.65
MPC		0.55
ClinPred		0.072	T
GERP RS		-4.8
Varity_R		0.13
gMVP		0.29

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

No publications associated with this variant yet.

Other links and lift over

hg19: chr11-2185556;