chr14-22548744-C-T

Variant names:

• chr14-22548744-C-T
• rs55766725
• ENST00000611116.2:c.272-894C>T

Variant summary

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

The ENST00000611116.2(TRAC):​c.272-894C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.823 in 147,296 control chromosomes in the GnomAD database, including 50,569 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 0.82 (50569 hom., cov: 21)
• Consequence: TRAC ENST00000611116.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.45
• Publications: 0 publications found

Genes affected

TRAC (HGNC:12029): (T cell receptor alpha constant) T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]

TRAC Gene-Disease associations (from GenCC):

• TCR-alpha-beta-positive T-cell deficiency

  Inheritance: AR, Unknown Classification: MODERATE, SUPPORTIVE, LIMITED Submitted by: Orphanet, Labcorp Genetics (formerly Invitae), PanelApp Australia, ClinGen

TRA (HGNC:12027):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.05).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.901 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000611116.2. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
There are no transcript annotations for this variant.

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	TRAC	ENST00000611116.2	TSL:6	c.272-894C>T		intron	N/A	ENSP00000480116.1	A0A5H1ZRS8

Frequencies

GnomAD3 genomes AF: 0.822 AC: 121058 AN: 147202 Hom.: 50524 Cov.: 21

Gnomad AFR AF: 0.909

Gnomad AMI AF: 0.878

Gnomad AMR AF: 0.801

Gnomad ASJ AF: 0.828

Gnomad EAS AF: 0.369

Gnomad SAS AF: 0.756

Gnomad FIN AF: 0.704

Gnomad MID AF: 0.813

Gnomad NFE AF: 0.830

Gnomad OTH AF: 0.837

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

GnomAD4 genome AF: 0.823 AC: 121152 AN: 147296 Hom.: 50569 Cov.: 21 AF XY: 0.813 AC XY: 58258 AN XY: 71654

African (AFR) AF: 0.909 AC: 36209 AN: 39840

American (AMR) AF: 0.801 AC: 11836 AN: 14780

Ashkenazi Jewish (ASJ) AF: 0.828 AC: 2845 AN: 3436

East Asian (EAS) AF: 0.369 AC: 1841 AN: 4988

South Asian (SAS) AF: 0.757 AC: 3483 AN: 4604

European-Finnish (FIN) AF: 0.704 AC: 6718 AN: 9544

Middle Eastern (MID) AF: 0.814 AC: 228 AN: 280

European-Non Finnish (NFE) AF: 0.830 AC: 55528 AN: 66928

Other (OTH) AF: 0.839 AC: 1679 AN: 2002

Alfa AF: 0.837 Hom.: 5770

Bravo AF: 0.830

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.1
CADD	Benign	1.7
PhyloP100		-1.4

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs55766725; hg19: chr14-23017690;