rs4926653

chr1-54730426-G-Achr1-54730426-G-C

Variant summary

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

The NM_004623.5(TTC4):c.682-1060G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.573 in 151,904 control chromosomes in the GnomAD database, including 25,739 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 0.57 (25739 hom., cov: 31)
• Consequence: TTC4 NM_004623.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.927

Genes affected

TTC4 (HGNC:12394): (tetratricopeptide repeat domain 4) This gene encodes a protein that contains tetratricopeptide (TPR) repeats, which often mediate protein-protein interactions and chaperone activity. The encoded protein interacts with heat shock proteins 70 and 90. Alternative splicing results in multiple transcript variants. Naturally-occuring readthrough transcription occurs from upstream gene MROH (maestro heat-like repeat family member 7) to this gene. [provided by RefSeq, Apr 2014]

MROH7-TTC4 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.94).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.943 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
TTC4	NM_004623.5	c.682-1060G>A		intron_variant		ENST00000371281.4
MROH7-TTC4	NR_037639.2	n.4860-1060G>A		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
TTC4	ENST00000371281.4	c.682-1060G>A		intron_variant		1	NM_004623.5	P1
TTC4	ENST00000371284.9	n.848-1060G>A		intron_variant, non_coding_transcript_variant		5

Frequencies

GnomAD3 genomes AF: 0.573 AC: 86897 AN: 151784 Hom.: 25718 Cov.: 31

Gnomad AFR AF: 0.610

Gnomad AMI AF: 0.651

Gnomad AMR AF: 0.578

Gnomad ASJ AF: 0.577

Gnomad EAS AF: 0.966

Gnomad SAS AF: 0.728

Gnomad FIN AF: 0.533

Gnomad MID AF: 0.535

Gnomad NFE AF: 0.513

Gnomad OTH AF: 0.552

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

GnomAD4 genome AF: 0.573 AC: 86970 AN: 151904 Hom.: 25739 Cov.: 31 AF XY: 0.577 AC XY: 42855 AN XY: 74220

Gnomad4 AFR AF: 0.610

Gnomad4 AMR AF: 0.578

Gnomad4 ASJ AF: 0.577

Gnomad4 EAS AF: 0.966

Gnomad4 SAS AF: 0.727

Gnomad4 FIN AF: 0.533

Gnomad4 NFE AF: 0.513

Gnomad4 OTH AF: 0.554

Alfa AF: 0.533 Hom.: 35857

Bravo AF: 0.580

Asia WGS AF: 0.807 AC: 2806 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
Cadd	Benign	6.8
Dann	Benign	0.74

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: rs4926653; hg19: chr1-55196099;