rs3766415

Variant names:

• chr1-54717459-A-G
• rs3766415
• NM_004623.5:c.230-33A>G

Variant summary

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

The NM_004623.5(TTC4):​c.230-33A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0656 in 1,462,854 control chromosomes in the GnomAD database, including 4,427 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 0.092 (919 hom., cov: 32)
  • Exomes 𝑓: 0.062 (3508 hom.)
• Consequence: TTC4 NM_004623.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.424
• Publications: 12 publications found

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:49180): (MROH7-TTC4 readthrough (NMD candidate)) This locus represents naturally occurring read-through transcription between the neighboring MROH7 (maestro heat-like repeat family member 7) and TTC4 (tetratricopeptide repeat domain 4) genes. Alternative splicing results in multiple transcript variants, which are candidates for nonsense-mediated mRNA decay (NMD) and are unlikely to produce protein products. [provided by RefSeq, Aug 2013]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.179 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_004623.5. 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
	TTC4	NM_004623.5	MANE Select	c.230-33A>G		intron	N/A	NP_004614.3
	TTC4	NM_001291333.2		c.230-33A>G		intron	N/A	NP_001278262.1
	MROH7-TTC4	NR_037639.2		n.4408-33A>G		intron	N/A

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	TTC4	ENST00000371281.4	TSL:1 MANE Select	c.230-33A>G		intron	N/A	ENSP00000360329.3	O95801
	MROH7-TTC4	ENST00000414150.6	TSL:2	n.3937-33A>G		intron	N/A	ENSP00000410192.2	A0A0A0MT08
	TTC4	ENST00000934475.1		c.230-33A>G		intron	N/A	ENSP00000604534.1

Frequencies

GnomAD3 genomes AF: 0.0921 AC: 14018 AN: 152138 Hom.: 915 Cov.: 32

Gnomad AFR AF: 0.171

Gnomad AMI AF: 0.0373

Gnomad AMR AF: 0.0505

Gnomad ASJ AF: 0.0403

Gnomad EAS AF: 0.139

Gnomad SAS AF: 0.191

Gnomad FIN AF: 0.0593

Gnomad MID AF: 0.0570

Gnomad NFE AF: 0.0520

Gnomad OTH AF: 0.0808

GnomAD2 exomes AF: 0.0791 AC: 12874 AN: 162714 AF XY: 0.0803

Gnomad AFR exome AF: 0.171

Gnomad AMR exome AF: 0.0361

Gnomad ASJ exome AF: 0.0414

Gnomad EAS exome AF: 0.143

Gnomad FIN exome AF: 0.0541

Gnomad NFE exome AF: 0.0544

Gnomad OTH exome AF: 0.0683

GnomAD4 exome AF: 0.0625 AC: 81909 AN: 1310598 Hom.: 3508 Cov.: 29 AF XY: 0.0650 AC XY: 41764 AN XY: 642196

African (AFR) AF: 0.172 AC: 4903 AN: 28500

American (AMR) AF: 0.0395 AC: 964 AN: 24430

Ashkenazi Jewish (ASJ) AF: 0.0399 AC: 791 AN: 19806

East Asian (EAS) AF: 0.145 AC: 5238 AN: 36112

South Asian (SAS) AF: 0.180 AC: 10228 AN: 56892

European-Finnish (FIN) AF: 0.0533 AC: 2580 AN: 48432

Middle Eastern (MID) AF: 0.0944 AC: 343 AN: 3632

European-Non Finnish (NFE) AF: 0.0509 AC: 52903 AN: 1039200

Other (OTH) AF: 0.0739 AC: 3959 AN: 53594

GnomAD4 genome AF: 0.0922 AC: 14040 AN: 152256 Hom.: 919 Cov.: 32 AF XY: 0.0946 AC XY: 7043 AN XY: 74462

African (AFR) AF: 0.171 AC: 7101 AN: 41530

American (AMR) AF: 0.0505 AC: 773 AN: 15300

Ashkenazi Jewish (ASJ) AF: 0.0403 AC: 140 AN: 3470

East Asian (EAS) AF: 0.139 AC: 721 AN: 5178

South Asian (SAS) AF: 0.189 AC: 914 AN: 4824

European-Finnish (FIN) AF: 0.0593 AC: 630 AN: 10620

Middle Eastern (MID) AF: 0.0544 AC: 16 AN: 294

European-Non Finnish (NFE) AF: 0.0520 AC: 3538 AN: 68014

Other (OTH) AF: 0.0818 AC: 173 AN: 2114

Alfa AF: 0.0663 Hom.: 1456

Bravo AF: 0.0912

Asia WGS AF: 0.167 AC: 581 AN: 3474

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	5.2
DANN	Benign	0.62
PhyloP100		-0.42
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.030		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: rs3766415; hg19: chr1-55183132; COSMIC: COSV64884466;