X-80022324-C-T

Position:

• chrX-80022324-C-T

Variant summary

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

The NM_001109878.2(TBX22):​c.55C>T​(p.Pro19Ser) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000000911 in 1,098,054 control chromosomes in the GnomAD database, with no homozygous occurrence. There are no hemizygote samples in GnomAD. In-silico tool predicts a benign outcome for this variant. 15/20 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).

• Frequency:
  • Genomes: not found (cov: 22)
  • Exomes 𝑓: 9.1e-7 (0 hom. 0 hem.)
• Consequence: TBX22 NM_001109878.2 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: -0.815

Genes affected

TBX22 (HGNC:11600): (T-box transcription factor 22) This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene have been associated with the inherited X-linked disorder, Cleft palate with ankyloglossia, and it is believed to play a major role in human palatogenesis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

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=0.03173524).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
TBX22	NM_001109878.2	c.55C>T	p.Pro19Ser	missense_variant	2/9	ENST00000373296.8	NP_001103348.1
TBX22	NM_016954.2	c.55C>T	p.Pro19Ser	missense_variant	1/8		NP_058650.1
TBX22	NM_001109879.2	c.-302C>T		5_prime_UTR_variant	2/9		NP_001103349.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
TBX22	ENST00000373296.8	c.55C>T	p.Pro19Ser	missense_variant	2/9	5	NM_001109878.2	ENSP00000362393.3
TBX22	ENST00000373294.8	c.55C>T	p.Pro19Ser	missense_variant	1/8	1		ENSP00000362390.5
TBX22	ENST00000476373.1	n.176C>T		non_coding_transcript_exon_variant	2/2	3
TBX22	ENST00000626498.2	n.55C>T		non_coding_transcript_exon_variant	2/9	2		ENSP00000487527.1

Frequencies

GnomAD3 genomes Cov.: 22

GnomAD4 exome AF: 9.11e-7 AC: 1 AN: 1098054 Hom.: 0 Cov.: 31 AF XY: 0.00 AC XY: 0 AN XY: 363416

Gnomad4 AFR exome AF: 0.00

Gnomad4 AMR exome AF: 0.00

Gnomad4 ASJ exome AF: 0.00

Gnomad4 EAS exome AF: 0.00

Gnomad4 SAS exome AF: 0.00

Gnomad4 FIN exome AF: 0.00

Gnomad4 NFE exome AF: 0.00000119

Gnomad4 OTH exome AF: 0.00

GnomAD4 genome Cov.: 22

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

Submissions by phenotype

Inborn genetic diseases Uncertain:1

Uncertain significance, criteria provided, single submitter

clinical testing

Ambry Genetics

Nov 15, 2021

The c.55C>T (p.P19S) alteration is located in exon 2 (coding exon 1) of the TBX22 gene. This alteration results from a C to T substitution at nucleotide position 55, causing the proline (P) at amino acid position 19 to be replaced by a serine (S). 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	0.098
BayesDel_addAF	Benign	-0.19	T
BayesDel_noAF	Benign	-0.50
CADD	Benign	0.43
DANN	Benign	0.79
DEOGEN2	Benign	0.049	T;T
FATHMM_MKL	Benign	0.087	N
M_CAP	Benign	0.0086	T
MetaRNN	Benign	0.032	T;T
MetaSVM	Benign	-0.92	T
MutationAssessor	Benign	0.58	N;N
PrimateAI	Benign	0.41	T
PROVEAN	Benign	-0.31	N;N
REVEL	Benign	0.20
Sift	Benign	0.50	T;T
Sift4G	Benign	0.68	T;T
Polyphen		0.0050	B;B
Vest4		0.14
MutPred		0.19		Gain of phosphorylation at P19 (P = 0.0126);Gain of phosphorylation at P19 (P = 0.0126);
MVP		0.28
MPC		0.16
ClinPred		0.030	T
GERP RS		-2.6
Varity_R		0.037
gMVP		0.48

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: rs1923747301; hg19: chrX-79277823;