chr1-118884605-GA-G

Variant names:

• chr1-118884605-GA-G
• rs536044359
• NM_001330677.2:c.*126delT

Variant summary

Our verdict is Benign. The variant received -10 ACMG points: 0P and 10B. BP6_Moderate BA1

The NM_001330677.2(TBX15):​c.*126delT variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0583 in 762,314 control chromosomes in the GnomAD database, including 47 homozygotes. Variant has been reported in ClinVar as Benign (★).

• Frequency:
  • Genomes: 𝑓 0.029 (47 hom., cov: 27)
  • Exomes 𝑓: 0.062 (0 hom.)
• Consequence: TBX15 NM_001330677.2 3_prime_UTR
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: 0.512
• Publications: 0 publications found

Genes affected

TBX15 (HGNC:11594): (T-box transcription factor 15) This gene belongs to the T-box family of genes, which encode a phylogenetically conserved family of transcription factors that regulate a variety of developmental processes. All these genes contain a common T-box DNA-binding domain. Mutations in this gene are associated with Cousin syndrome.[provided by RefSeq, Oct 2009]

TBX15 Gene-Disease associations (from GenCC):

• pelviscapular dysplasia

  Inheritance: AR Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: G2P, Labcorp Genetics (formerly Invitae), Orphanet

ACMG classification

Our verdict: Benign. The variant received -10 ACMG points.

• BP6: Variant 1-118884605-GA-G is Benign according to our data. Variant chr1-118884605-GA-G is described in ClinVar as Benign. ClinVar VariationId is 1243200.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.0703 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TBX15	NM_001330677.2	c.*126delT		3_prime_UTR_variant	Exon 8 of 8	ENST00000369429.5	NP_001317606.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TBX15	ENST00000369429.5	c.*126delT		3_prime_UTR_variant	Exon 8 of 8	5	NM_001330677.2	ENSP00000358437.3
TBX15	ENST00000207157.7	c.*126delT		3_prime_UTR_variant	Exon 8 of 8	1		ENSP00000207157.3
TBX15	ENST00000449873.5	c.*126delT		3_prime_UTR_variant	Exon 4 of 4	5		ENSP00000398625.1

Frequencies

GnomAD3 genomes AF: 0.0289 AC: 2334 AN: 80746 Hom.: 47 Cov.: 27

Gnomad AFR AF: 0.0729

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.0184

Gnomad ASJ AF: 0.0109

Gnomad EAS AF: 0.0124

Gnomad SAS AF: 0.00399

Gnomad FIN AF: 0.00315

Gnomad MID AF: 0.00833

Gnomad NFE AF: 0.00380

Gnomad OTH AF: 0.0219

GnomAD4 exome AF: 0.0617 AC: 42074 AN: 681548 Hom.: 0 Cov.: 6 AF XY: 0.0611 AC XY: 21307 AN XY: 348734

⚠️ The allele balance in gnomAD version 4 Exomes is significantly skewed from the expected value of 0.5.

African (AFR) AF: 0.0794 AC: 1283 AN: 16156

American (AMR) AF: 0.0581 AC: 1076 AN: 18520

Ashkenazi Jewish (ASJ) AF: 0.0629 AC: 912 AN: 14502

East Asian (EAS) AF: 0.0762 AC: 2229 AN: 29262

South Asian (SAS) AF: 0.0430 AC: 2066 AN: 48054

European-Finnish (FIN) AF: 0.0604 AC: 1718 AN: 28442

Middle Eastern (MID) AF: 0.0627 AC: 144 AN: 2298

European-Non Finnish (NFE) AF: 0.0621 AC: 30546 AN: 491904

Other (OTH) AF: 0.0648 AC: 2100 AN: 32410

⚠️ The allele balance in gnomAD4 Exomes is highly skewed from 0.5 (p-value = 0), which strongly suggests a high chance of mosaicism in these individuals.

GnomAD4 genome AF: 0.0289 AC: 2336 AN: 80766 Hom.: 47 Cov.: 27 AF XY: 0.0285 AC XY: 1079 AN XY: 37854

African (AFR) AF: 0.0729 AC: 1985 AN: 27212

American (AMR) AF: 0.0182 AC: 124 AN: 6822

Ashkenazi Jewish (ASJ) AF: 0.0109 AC: 21 AN: 1932

East Asian (EAS) AF: 0.0124 AC: 27 AN: 2172

South Asian (SAS) AF: 0.00397 AC: 8 AN: 2014

European-Finnish (FIN) AF: 0.00315 AC: 10 AN: 3176

Middle Eastern (MID) AF: 0.00877 AC: 1 AN: 114

European-Non Finnish (NFE) AF: 0.00380 AC: 136 AN: 35824

Other (OTH) AF: 0.0220 AC: 24 AN: 1092

Alfa AF: 0.00 Hom.: 6

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Nov 22, 2019

GeneDx

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

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Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
PhyloP100		0.51
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: rs536044359; hg19: chr1-119427228;