rs6091653

chr20-53257173-T-C

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_173485.6(TSHZ2):c.*8+602T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.113 in 152,302 control chromosomes in the GnomAD database, including 1,087 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 0.11 (1087 hom., cov: 33)
• Consequence: TSHZ2 NM_173485.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.19

Genes affected

TSHZ2 (HGNC:13010): (teashirt zinc finger homeobox 2) This gene is a member of the teashirt C2H2-type zinc-finger protein family of transcription factors. This gene encodes a protein with five C2H2-type zinc fingers, a homeobox DNA-binding domain and a coiled-coil domain. This nuclear protein is predicted to act as a transcriptional repressor. This gene is thought to play a role in the development and progression of breast and other types of cancer. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]

(HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.136 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
TSHZ2	NM_173485.6	c.*8+602T>C		intron_variant		ENST00000371497.10

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
TSHZ2	ENST00000371497.10	c.*8+602T>C		intron_variant		1	NM_173485.6	P1
	ENST00000606932.1	n.140-610A>G		intron_variant, non_coding_transcript_variant		5
TSHZ2	ENST00000603338.2	c.*8+602T>C		intron_variant		2
TSHZ2	ENST00000605656.2	c.*8+602T>C		intron_variant, NMD_transcript_variant		4

Frequencies

GnomAD3 genomes AF: 0.113 AC: 17243 AN: 152184 Hom.: 1084 Cov.: 33

Gnomad AFR AF: 0.139

Gnomad AMI AF: 0.0691

Gnomad AMR AF: 0.0846

Gnomad ASJ AF: 0.0957

Gnomad EAS AF: 0.000962

Gnomad SAS AF: 0.0352

Gnomad FIN AF: 0.0986

Gnomad MID AF: 0.117

Gnomad NFE AF: 0.122

Gnomad OTH AF: 0.120

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

GnomAD4 genome AF: 0.113 AC: 17258 AN: 152302 Hom.: 1087 Cov.: 33 AF XY: 0.109 AC XY: 8125 AN XY: 74488

Gnomad4 AFR AF: 0.139

Gnomad4 AMR AF: 0.0845

Gnomad4 ASJ AF: 0.0957

Gnomad4 EAS AF: 0.000964

Gnomad4 SAS AF: 0.0352

Gnomad4 FIN AF: 0.0986

Gnomad4 NFE AF: 0.122

Gnomad4 OTH AF: 0.119

Alfa AF: 0.116 Hom.: 1521

Bravo AF: 0.111

Asia WGS AF: 0.0270 AC: 95 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
Cadd	Benign	0.44
Dann	Benign	0.40

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs6091653; hg19: chr20-51873712;